Treatment of pulmonary and other conditions

ABSTRACT

Disclosed is a compound, or a pharmaceutically acceptable salt or ester thereof, having a structure of: 
       X 1 -L-X 2    
     wherein L is a linking moiety comprising an enone; and
 
X 1  and X 2  are each independently an optionally-substituted N-heterocycle.
 
     Also disclosed are method for treating pulmonary conditions and other organ or system conditions with the compounds.

This application claims the benefit of U.S. Provisional Application No.61/822,224, filed May 10, 2013, which is incorporated herein byreference in its entirety.

ACKNOWLEDGMENT OF GOVERNMENT SUPPORT

This invention was made with government support under grant numberHL093196 awarded by National Institutes of Health. The government hascertain rights in the invention.

BACKGROUND

The lung is an organ that is dependent on delicate structures such asthe alveolar-capillary interface for its crucial gas-exchange function,yet is routinely exposed to toxins and irritants in the inspired air. Itcan also be injured by toxins and inflammatory products generated byinfections and derangements elsewhere in the body. It is thus subject toa wide variety of diseases, for many of which the pathogenesis isincompletely known. Some of these diseases and conditions have effectivetreatments available; these treatments may include administration ofsteroids, other anti-inflammatory agents, small molecules, ortherapeutic antibodies. However, for some diseases and conditions andsubsets of patients with other conditions, efficacy of all availabletreatments is limited. The most commonly employed treatment in manycases is corticosteroid administration, which is often associated withsignificant adverse effects.

Pulmonary fibrosis is a lung disease that can result from exposure toradiation, from infections, from inflammatory processes, or fromautoimmune disorders. In other cases, known as idiopathic pulmonaryfibrosis (IPF), the cause is unknown. Regardless of the triggeringinsult, the outcome is uncontrollable inflammation, immune activity,lung injury/repair, and fibrotic processes that damage the lung. Thescarring of the lungs that occurs in these diseases reduces the abilityof the lungs to transfer oxygen into the blood, causing hypoxemia. Aprimary aim of a treatment for pulmonary fibrosis is to reduceinflammation and injury and enhance lung repair, and thus to halt theabnormal processes that result in irreversible fibrosis. Currentlyavailable therapies for pulmonary fibrosis are very limited.

Chronic obstructive pulmonary disease (COPD) is a growing problem.Patients present with symptoms of cough, excessive production of mucus,and dyspnea that may be connected with bronchitis or emphysema. Whilebronchitis represents inflammation of the airways, emphysema is a moreadvanced disease representing destruction of the lung parenchyma byoxidants and proteases released as part of the inflammatory process.Development of COPD is most often attributed to smoking or exposure toenvironmental toxins over a period of many years, although the diseasecontinues to progress even after smoking cessation. The pathophysiologyin COPD also features “steroid resistance,” mediated by reduced HDAC(histone deacetylase) enzyme activity. As a result, the most commonlyused anti-inflammatory drug has little effect and is incapable ofhalting progression. The only treatment available for COPD isadministration of drugs that alleviate the symptoms.

A pulmonary disease with symptoms often overlapping those of COPD isasthma. Airway inflammation in asthma is characterized by activation ofa variety of immune-system cells. Asthma pathology features increasedproduction of a number of cytokines, primarily of the Th2 classassociated with adaptive immunity, together with tissue eosinophilia andincreased IgE production. A diagnostic feature of asthma is excessiveresponse of the airways to bronchoconstrictors such as methacholine. Themost effective therapy for asthma remains corticosteroids, typicallyadministered by inhalation. Bronchodilators are also employed,frequently in combination with corticosteroids. Some patients, however,exhibit “steroid resistant” asthma that does not respond tocorticosteroids.

Cystic fibrosis is a genetic disease affecting a chloride ion channel inthe membrane of epithelial cells. Failure of chloride ion transportresults in production of thick, viscous secretions. Mucus production inthe lungs is among the many secretions affected. A prominent feature ofcystic fibrosis is inflammation that is only partially due to thefrequent infections that are also a feature of the disease. Thisneutrophil-rich inflammation is one factor in the gradual loss of lungfunction that eventually leads to death. Therapies involved inattenuating lung function decline are limited.

ALI (acute lung injury) and ARDS (acute respiratory distress syndrome)are lung diseases that can result from a wide variety of injuries eitherintrinsic or extrinsic to the lung. In the acute phase there issloughing of both bronchial and alveolar epithelial cells, withformation of protein-rich hyaline membranes on the denuded basementmembrane. This leads to inflammation, with neutrophils adhering to theinjured capillary endothelium and migrating through the interstitiuminto the air space. In the air space, alveolar macrophages secretepro-inflammatory cytokines, which act locally to stimulate chemotaxisand activate neutrophils that release oxidants, proteases, leukotrienes,and other proinflammatory molecules, such as platelet-activating factor.The oxidants and proteases produce more injury, and the cycle continues.There is no approved pharmacological therapy for ALI/ARDS.

Ischemia-reperfusion injury occurs when blood flow returns to an organthat has been starved of oxygen. Ischemia followed by reperfusion isinevitable in organ transplantation but also accompanies such conditionsas myocardial infarction and stroke. The mechanisms involved are complexbut involvement of inflammation and associated production of reactiveoxygen species is common Reactive oxygen species are strong oxidantsthat can damage components of many cells. Organs can only withstand alimited period of ischemia before suffering injury on reperfusion.Attempts to extend this period by treatments prior to transplantationhave had limited success and post-transplantation treatments appear evenless useful. The most effective current method for extending thepermissible period of ischemia is by reducing the organ's metabolic rateduring the period between harvest and reimplantation.

Pulmonary hypertension is defined as abnormally high blood pressurespecifically in the vasculature of the lungs. It is usually secondary toconditions that limit pulmonary blood flow or oxygenation but may alsooccur without identifiable cause. A key feature of the pathogenesis isabnormal proliferation of vascular cells together with failure ofappropriate apoptosis. Current management focuses on vasodilators andsymptom-reducing strategies, but compounds that block cell proliferationand other pathways are now being investigated.

Lung cancer is the leading cause of cancer death in the US, with only16% of patients diagnosed with lung cancer surviving as much as fiveyears. It is estimated that 80%-90% of all lung cancers are the resultof cigarette smoke. Like other environmental carcinogens, which may alsoinduce lung cancer, the carcinogens in cigarette smoke cause mutationsthat lead to uncontrolled proliferation of the affected cells and alsoallow them to invade normal tissues. Treatments are surgery, radiation,and chemotherapy, with the choice depending to some extent on thespecific type of cancer involved, but only surgical removal of a tumorthat has not yet spread provides any hope for long-term survival. As thepoor long-term survival statistics indicate, better treatments areneeded.

SUMMARY

One embodiment disclosed herein relates to a compound, or apharmaceutically acceptable salt or ester thereof,

having a structure of:

X¹-L-X²

wherein L is a linking moiety comprising an enone; andX¹ and X² are each independently an optionally-substitutedN-heterocycle.

A further embodiment disclosed herein relates to a compound, or apharmaceutically acceptable salt or ester thereof, comprising an adductof a hydrophilic thiol and an enone that comprises at least twoN-heterocycles.

An additional embodiment disclosed herein relates to a compound, or apharmaceutically acceptable salt or ester thereof, having a structureof:

wherein

represents a single bond or a double bond;A is CH if

is a double bond, or CH(S—R⁵) if

is a single bond, wherein R⁵ is a peptide, amino acid, amino acidderivative, optionally-substituted alkyl, optionally-substitutedalkenyl, optionally-substituted alkynyl, optionally-substitutedcycloalkyl, or optionally-substituted cycloalkenyl; andX¹ and X² are each independently an optionally-substitutedN-heterocycle; or

wherein

represents a single bond or a double bond;A is CH if

is a double bond, or CH(S—R⁵) if

is a single bond, wherein R⁵ is a peptide, amino acid, amino acidderivative, optionally-substituted alkyl, optionally-substitutedalkenyl, optionally-substituted alkynyl, optionally-substitutedcycloalkyl, or optionally-substituted cycloalkenyl;X¹ and X² are each independently an optionally-substitutedN-heterocycle; andR¹, R², and R³ are each independently C or N; or

wherein

represents a single bond or a double bond;A is CH if

is a double bond, or CH(S—R⁵) if

is a single bond, wherein R⁵ is a peptide, amino acid, amino acidderivative, optionally-substituted alkyl, optionally-substitutedalkenyl, optionally-substituted alkynyl, optionally-substitutedcycloalkyl, or optionally-substituted cycloalkenyl;X¹ and X² are each independently an optionally-substitutedN-heterocycle; and

R¹ is C or N; or

wherein

represents a single bond or a double bond;A is CH if

is a double bond, or CH(S—R⁵) if

is a single bond, wherein R⁵ is a peptide, amino acid, amino acidderivative, optionally-substituted alkyl, optionally-substitutedalkenyl, optionally-substituted alkynyl, optionally-substitutedcycloalkyl, or optionally-substituted cycloalkenyl;R¹ and R² are each independently C or N; andX¹ and X² are each independently an optionally-substitutedN-heterocycle.

Also disclosed herein are pharmaceutical compositions comprising acompound disclosed herein, and at least one pharmaceutically acceptableexcipient.

Further disclosed is a method for treating a pulmonary disease in asubject comprising administering to the subject in need thereof atherapeutically effective amount of a compound or pharmaceuticalcomposition disclosed herein.

Additionally disclosed is a method for treating an ischemia-reperfusioncondition in a subject comprising administering to the subject in needthereof a therapeutically effective amount of a compound orpharmaceutical composition disclosed herein.

Also disclosed herein is a method of inhibiting NF-κB activity in asubject, comprising administering to the subject in need thereof aninhibitory amount of a compound or pharmaceutical composition disclosedherein.

Further disclosed herein is a method of inhibiting lung fibroblastproliferation in a subject, comprising administering to the subject inneed thereof an inhibitory amount of a compound or pharmaceuticalcomposition disclosed herein.

Additionally disclosed herein is a method of inhibiting myofibroblastdifferentiation in a subject, comprising administering to the subject inneed thereof an inhibitory amount of a compound or pharmaceuticalcomposition disclosed herein.

Also disclosed herein is a method of inhibiting an oxidizing agent inlung tissue of a subject, comprising administering to the subject inneed thereof a therapeutically effective amount of a compound orpharmaceutical composition disclosed herein.

Further disclosed herein is a method of ameliorating or preventing acuteor chronic rejection of a transplanted organ in a subject, comprisingadministering to the subject in need thereof a therapeutically effectiveamount of a compound or pharmaceutical composition disclosed herein.

Additionally disclosed herein is a method for increasing a subject'sendogenous antioxidant activity via upregulation of the activity of thetranscription factor Nrf2, comprising administering to the subject inneed thereof a therapeutically effective amount of a compound orpharmaceutical composition disclosed herein.

Also disclosed herein is a method for inhibiting pulmonary collagendeposition in a subject, comprising administering to the subject in needthereof a therapeutically effective amount of a compound orpharmaceutical composition disclosed herein.

Further disclosed herein is a method for decreasing proliferation andinducing apoptosis in lung cancer cells, comprising contacting the cellswith an effective amount of a compound or pharmaceutical compositiondisclosed herein.

Additionally disclosed herein is method for improving the phagocytoticability of alveolar macrophages, comprising contacting the microphageswith an effective amount of a compound or pharmaceutical compositiondisclosed herein.

Also disclosed herein is a method for diminishing the inflammatoryresponse to allergen in a subject, comprising administering to thesubject in need thereof a therapeutically effective amount of a compoundor pharmaceutical composition disclosed herein.

Further disclosed herein is a method for diminishing the inflammatoryresponse to an inflammatory, irritating, or cytotoxic agent in asubject, comprising administering to the subject in need thereof atherapeutically effective amount of a compound or pharmaceuticalcomposition disclosed herein.

Additionally disclosed herein is a method for diminishingallergen-induced excessive response to bronchoconstrictors (e.g.,methacholine) in a subject, comprising administering to the subject inneed thereof a therapeutically effective amount of a compound orpharmaceutical composition disclosed herein.

Also disclosed herein is a method for diminishing allergen-inducedairway remodeling in a subject, comprising administering to the subjectin need thereof a therapeutically effective amount of a compound orpharmaceutical composition disclosed herein.

Further disclosed herein is a method for diminishing hypoxia-inducedremodeling of the pulmonary vasculature in a subject, comprisingadministering to the subject in need thereof a therapeutically effectiveamount of a compound or pharmaceutical composition disclosed herein.

The foregoing will become more apparent from the following detaileddescription, which proceeds with reference to the accompanying figures.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 demonstrates nebulization of PB141. PB141 was dissolved in wateror different concentrations of PBS and the solutions were aerosolizedusing a micropump nebulizer (Buxco Research Systems, Wilmington, N.C.)flowing at 10 L of air/min. Aerosol droplet size was measured with anAndersen cascade impactor. (A) Distribution of PB141 aerosol dropletsizes. (B) The concentration of PB141 during a 30 min nebulizationperiod was measured by collecting samples during nebulization andanalyzing by spectrophotometer in two independent experiments.

FIG. 2 shows that PB141 exhibits anti-oxidant activities. Theanti-oxidant activities of PB 141 were determined by the ability of thiscompound to react with pre-formed radical monocation of2,2′-azinobis-(3-ethylbenzothiazoline)-6-sulfonic acid (ABTS⁺). Data arerepresentative of one of two independent experiments; n=3; *** P<0.001versus Troxol.

FIG. 3 shows that PB141 exhibits anti-oxidant activities. Theantioxidant activity of PB141 was determined by ferricreduction/anti-oxidant power (FRAP) assay in which the compound isreacted with ferric tripyridyltriazine complex. Data are representativeof one of two independent experiments; n=3; *** P<0.001 versus Troxol.

FIG. 4 shows that PB141 is rapidly cleared from the systemiccirculation. After pulmonary delivery of PB141 for 7 days, blood wascollected at intervals from the retro-orbital plexus and plasmaseparated. Plasma PB141 was determined by isocratic HPLC.

FIG. 5 demonstrates absence of kidney, liver or lung toxicity followinglong-term, high-dose pulmonary delivery of PB141. PB141 was delivered tomice by nebulization at doses of 25 or 250 mg/kg for up to 30 days. (A)Lungs were excised, sectioned, and examined histologically for evidenceof inflammation or injury. (B) Potential kidney and liver injury wereassessed by serum levels of creatinine, AST, and ALT. (C) Shows thatnebulized PB141 inhibits LPS-induced upregulation of NF-κB in aconcentration-dependent manner. Acute lung injury was induced in mice byintratracheal administration of LPS. Thirty min later PBS or varyingconcentrations of PB141 were delivered into cage air by nebulization.Following sacrifice, nuclear proteins were isolated from lungs and usedto determine DNA-binding activity of the p65 subunit of thepro-inflammatory transcription factor NF-κB.

FIG. 6 shows that PB141 treatment in vitro upregulates Nrf2 and inhibitsNF-κB activity. BEAS-2B cells were treated with varying concentrationsof PB141 for 24 h, after which (A) Nrf2 activity was measured or (C)nuclear Nrf2 concentration was determined by Western blotting. (B) Inother experiments cells were pretreated with varying concentrations ofPB141 for 1 h, then with LPS (500 ng/ml) for 6 h. Cells were thenisolated and activity of NF-κB was measured.

FIG. 7 shows that PB141 inhibits lung fibroblast proliferation. IMR-90cells were cultured in Dulbecco's modified Eagle's medium (DMEM)containing 10% heat-inactivated fetal bovine serum, penicillin, andstreptomycin (100 IU/ml). Monolayer cultures were deprived of serum for24 h, and treated with different concentrations of PB141 for differenttime periods as indicated. Cell numbers were then counted at 24, 48, and72 h. Data are representative of one of two independent experiments;n=3.

FIG. 8 shows that PB141 inhibits TGF-β-induced myofibroblastdifferentiation. IMR-90 cells were cultured in Dulbecco's modifiedEagle's medium (DMEM) containing 10% heat-inactivated fetal bovineserum, penicillin, and streptomycin (100 IU/ml). Monolayer cultures weredeprived of serum for 24 h, pre-treated with 0.5 μM PB141 or withvehicle (saline) for 1 h, and then exposed to 2 ng/ml TGF-β for 24 h.(A) Western blot analysis for α-smooth muscle actin. (B) Quantitativevalues for each condition. ***P<0.001 vs Veh. (C) Immunofluorescencemicroscopy for α-SMA following treatment. Blots and images arerepresentative of two independent experiments.

FIG. 9 shows that nebulized PB141 reduces bleomycin-induced pulmonaryfibrosis. Induction of pulmonary fibrosis by intratracheal injection ofbleomycin sulphate (BLM; 0.05 units) was followed by nebulization ofPB141 (25 mg/kg) or vehicle (saline) and delivery to cage air via amicropump nebulizer. After 21 days lung samples were obtained. (A) Lunghydroxyproline content. (B) Lung fibrinolysis. (C) Lung collagencontent. (D) Lung TGF-β content. Data are representative of one of twoindependent experiments with n=5-7 mice per group; ** p<0.01, ***p<0.001.

FIG. 10 shows that nebulized PB141 reduces LPS-induced lung inflammationand oxidative damage. Induction of ALI by intratracheal injection of LPS(50 μg) was followed 30 min later by nebulization of PB141 (25 mg/kg) orvehicle (saline) and delivery to cage air via a micropump nebulizer.After a further 5.5 h, BAL fluid, plasma, and lung samples wereobtained. (A) Total cell and (B) neutrophil number in BAL fluid;myeloperoxidase activity in (C) lung tissue and (D) BAL fluid; (E)microscopic examination following staining of BAL fluid; (F) H₂O₂production; (G) nitrate concentration, and (H) malonyldialdehyde/proteinratio in lung. Plasma levels of (I) MIP-2, (J) IL-6, (K) TNF-α, and (L)KC. Data are representative of one of two independent experiments withn=5-8 mice per group; *** p<0.001.

FIG. 11 shows that nebulized PB141 reduces LPS-induced lung injury.Induction of ALI by intratracheal injection of LPS (50 μg) was followed30 min later by nebulization of PB141 (25 mg/kg) or vehicle (saline) anddelivery to cage air via a micropump nebulizer. After a further 5.5 h,BAL fluid and lung samples were obtained. (A) Protein concentration inBAL fluid. (B) Ratio of lung wet:dry weight. (C) Histologicalexamination of the lung following H&E staining. Data are representativeof one of two independent experiments with n=5-8 mice per group; ***p<0.001.

FIG. 12 shows that PB141 reverses the LPS-induced decrease intranscription factor Nrf2 activity. Induction of ALI by intratrachealinjection of LPS (50 μg) was followed 30 min later by nebulization ofPB141 (25 mg/kg) or vehicle (saline) and delivery to cage air via amicropump nebulizer. After another 5.5 h lungs were excised andDNA-binding activity of the transcription factor Nrf2 was determined.Data is representative of one of two independent experiments with n=4-6mice per group; *** p<0.001.

FIG. 13 shows that PB141 reduces inflammatory gene and increasesantioxidant gene transcription in LPS-activated alveolar macrophages.Induction of ALI by intratracheal injection of LPS (50 μg) was followed30 min later by nebulization of PB141 (25 mg/kg) or vehicle (saline) anddelivery to cage air via a micropump nebulizer. After another 5.5 h BALfluid was obtained. Alveolar macrophages were isolated from the BALfluid and plated in DMEM+10% FBS. After 1 h, RNA was isolated andexpression of the indicated genes was determined using real-time PCR;results were normalized to values for the housekeeping genesglyceraldehyde-3-phosphate dehydrogenase (GAPDH) and 9s rRNA. Data arerepresentative of one of two independent experiments with n=6-8 mice pergroup; **P<0.01; ***P<0.001.

FIG. 14 shows that nebulized PB141 reduces4-methylnitrosamino-1-(3-pyridyl)-1-butanone (NNK)-induced lungtumorigenesis in A/J mice. Induction of lung tumorigenesis byintraperitoneal (i.p.) injection on days 1, 3, and 5 with 50 mg/kg ofNNK dissolved in saline was followed by nebulization of PB141 (25 mg/kg)or vehicle (saline) and delivery to cage air via a micropump nebulizer.After 8 weeks the lung was examined histologically following H&Estaining. (A) Number of lung lesions. (B) Histology showing lung tumorincidence and burden. Data are representative of one of two independentexperiments with n=9-11 mice per group.

FIG. 15 shows that nebulized PB141 reduces ovalbumin (OVA)-inducedairway hyperresponsiveness. Allergen-induced asthma was produced in miceby initial sensitization by intraperitoneal (i.p.) injection of OVA ondays 0 and 7 and challenge by intratracheal injection of OVA oneven-numbered days 14 through 22. Thirty minutes following each OVAchallenge, PB141 (25 mg/kg) or vehicle (saline) was nebulized anddelivered to cage air via a micropump nebulizer. Twenty-four hours afterthe last challenge and nebulization; airway hyperresponsiveness toincreasing concentrations of inhaled methacholine was determined by theforced oscillation (flexiVent) method. (A) Airway resistance. (B) Airwayelastance. Data are representative of one of two independent experimentswith n=6-8 mice per group.

FIG. 16 shows that nebulized PB141 reduces ovalbumin (OVA)-induced lunginflammation and oxidative damage. Allergen induced asthma was producedin mice by initial sensitization by intraperitoneal (i.p.) injection ofOVA on days 0 and 7 and challenge by intratracheal injection of OVA oneven-numbered days 14 through 22. Thirty minutes after each OVAchallenge, PB141 (25 mg/kg) or vehicle (saline) was nebulized anddelivered to cage air via a micropump nebulizer. Twenty-four hoursfollowing the last challenge and nebulization, BAL fluid, plasma, andlung samples were obtained. (A) Total and differential cell count in BALfluid. (B) Microscopic examination following staining of BAL fluid. (C)H₂O₂ production, (D) Protein concentration in BAL fluid. Data arerepresentative of one of two independent experiments with n=7-10 miceper group; *** p<0.001.

FIG. 17 shows that nebulized PB141 reduces ovalbumin (OVA)-inducedinflammatory cell infiltration and mucus production. Allergen-inducedasthma was produced in mice by initial sensitization by intraperitoneal(i.p.) injection of OVA on days 0 and 7 and challenge by intrachealinjection of OVA on even-numbered days 14 through 22. Thirty minutesafter each OVA challenge, PB141 (25 mg/kg) or vehicle (saline) wasnebulized and delivered to cage air via a micropump nebulizer.Twenty-four hours following the last challenge and nebulization lungsamples were obtained. The lung was examined histologically following(A) H&E staining, (B) trichrome staining, and (C) periodic acid Schiffs(PAS) staining. Data are representative of one of two independentexperiments with n=7-10 mice per group.

FIG. 18 shows that nebulized PB141 reduces infiltration ofinflammation-related cells into pulmonary spaces and production ofinflammatory mediators in a murine model of chronic obstructivepulmonary disease (COPD). COPD was induced by exposure of mice towhole-body cigarette smoke for 5 days, at the end of which the mice wereeuthanized and cells and levels of mediators were obtained from thepulmonary airspace by bronchoalveolar lavage. Some mice received PB141(25 mg/kg) simultaneously with the cigarette smoke (A-I).

FIG. 19 shows that nebulized PB141 reduces chronic hypoxia (CH)-inducedpulmonary hypertension and right ventricular hypertrophy. CH-inducedpulmonary hypertension was produced in mice by exposing them to chronichypoxia (CH; FI_(O2) 10%) or room air (N; control) for 3 weeks. Duringthe last 10 days of exposure, PB141 (25 mg/kg) or vehicle (saline) wasnebulized and delivered to cage air via a micropump nebulizer.Twenty-four hours following the last nebulization mice were anesthetizedand the right internal jugular vein of each mouse was surgically exposedand cannulated with a pressure transducer that was advanced to recordright ventricular pressure, then advanced further to measure pulmonaryarterial pressure: (top left) mean pulmonary arterial pressure; (topright) right ventricular systolic pressure (RVSP); (bottom left)peripheral vascular resistance; (bottom right) right ventricularhypertrophy. Data are representative of one of two independentexperiments with n=4-6 mice per group.

FIG. 20 shows that nebulized PB141 reduces chronic hypoxia (CH)-inducedpulmonary hypertension and vascular remodeling. CH-induced pulmonaryhypertension was produced in mice by exposing them to CH (FI_(O2) 10%)or room air for 3 weeks. During the last 10 days of exposure, PB141 (25mg/kg) or vehicle (saline) was nebulized and delivered to cage air via amicropump nebulizer. Twenty-four hours following the last nebulizationlung samples were obtained. Graphs show medial wall thickness ofa-SMA-positive acinar blood vessels and percent of non-muscularized,partially muscularized, and fully muscularized small vessels. Data arerepresentative of one of two independent experiments with n=4-6 mice pergroup.

FIG. 21 shows the proposed mechanism of action of PB141.

DETAILED DESCRIPTION Terminology

The following explanations of terms and methods are provided to betterdescribe the present compounds, compositions and methods, and to guidethose of ordinary skill in the art in the practice of the presentdisclosure. It is also to be understood that the terminology used in thedisclosure is for the purpose of describing particular embodiments andexamples only and is not intended to be limiting.

“Acyl” refers to a group having the structure —C(O)R, where R may be,for example, optionally substituted alkyl, optionally substituted aryl,or optionally substituted heteroaryl. “Lower acyl” groups are those thatcontain one to six carbon atoms. Acetyl is an example of an acyl.

“Acyloxy” refers to a group having the structure —OC(O)R—, where R maybe, for example, optionally substituted alkyl, optionally substitutedaryl, or optionally substituted heteroaryl. “Lower acyloxy” groupscontain one to six carbon atoms.

“Administration” as used herein is inclusive of administration byanother person to the subject or self-administration by the subject.

The term “aliphatic” is defined as including alkyl, alkenyl, alkynyl,halogenated alkyl and cycloalkyl groups. A “lower aliphatic” group is abranched or unbranched aliphatic group having from 1 to 10 carbon atoms.

“Alkanediyl,” “cycloalkanediyl,” “aryldiyl,” “alkanearyldiyl” refers toa divalent radical derived from aliphatic, cycloaliphatic, aryl, andalkanearyl hydrocarbons.

“Alkenyl” refers to a cyclic, branched or straight chain groupcontaining only carbon and hydrogen, and contains one or more doublebonds that may or may not be conjugated. Alkenyl groups may beunsubstituted or substituted. “Lower alkenyl” groups contain one to sixcarbon atoms.

The term “alkoxy” refers to a straight, branched or cyclic hydrocarbonconfiguration and combinations thereof, including from 1 to 20 carbonatoms, preferably from 1 to 8 carbon atoms (referred to as a “loweralkoxy”), more preferably from 1 to 4 carbon atoms, that include anoxygen atom at the point of attachment. An example of an “alkoxy group”is represented by the formula —OR, where R can be an alkyl group,optionally substituted with an alkenyl, alkynyl, aryl, aralkyl,cycloalkyl, halogenated alkyl, alkoxy or heterocycloalkyl group.Suitable alkoxy groups include methoxy, ethoxy, n-propoxy, i-propoxy,n-butoxy, i-butoxy, sec-butoxy, tert-butoxy cyclopropoxy, cyclohexyloxy,and the like.

“Alkoxycarbonyl” refers to an alkoxy substituted carbonyl radical,—C(O)OR, wherein R represents an optionally substituted alkyl, aryl,aralkyl, cycloalkyl, cycloalkylalkyl or similar moiety.

The term “alkyl” refers to a branched or unbranched saturatedhydrocarbon group of 1 to 24 carbon atoms, such as methyl, ethyl,n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, hexyl, heptyl,octyl, decyl, tetradecyl, hexadecyl, eicosyl, tetracosyl and the like. A“lower alkyl” group is a saturated branched or unbranched hydrocarbonhaving from 1 to 6 carbon atoms. Preferred alkyl groups have 1 to 4carbon atoms. Alkyl groups may be “substituted alkyls” wherein one ormore hydrogen atoms are substituted with a substituent such as halogen,cycloalkyl, alkoxy, amino, hydroxyl, aryl, alkenyl, or carboxyl. Forexample, a lower alkyl or (C₁-C₆)alkyl can be methyl, ethyl, propyl,isopropyl, butyl, iso-butyl, sec-butyl, pentyl, 3-pentyl, or hexyl;(C₃-C₆)cycloalkyl can be cyclopropyl, cyclobutyl, cyclopentyl, orcyclohexyl; (C₃-C₆)cycloalkyl(C₁-C₆)alkyl can be cyclopropylmethyl,cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl,2-cyclopropylethyl, 2-cyclobutylethyl, 2-cyclopentylethyl, or2-cyclohexylethyl; (C₁-C₆)alkoxy can be methoxy, ethoxy, propoxy,isopropoxy, butoxy, iso-butoxy, sec-butoxy, pentoxy, 3-pentoxy, orhexyloxy; (C₂-C₆)alkenyl can be vinyl, allyl, 1-propenyl, 2-propenyl,1-butenyl, 2-butenyl, 3-butenyl, 1,-pentenyl, 2-pentenyl, 3-pentenyl,4-pentenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, or 5-hexenyl;(C₂-C₆)alkynyl can be ethynyl, 1-propynyl, 2-propynyl, 1-butynyl,2-butynyl, 3-butynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl,1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, or 5-hexynyl;(C₁-C₆)alkanoyl can be acetyl, propanoyl or butanoyl; halo(C₁-C₆)alkylcan be iodomethyl, bromomethyl, chloromethyl, fluoromethyl,trifluoromethyl, 2-chloroethyl, 2-fluoroethyl, 2,2,2-trifluoroethyl, orpentafluoroethyl; hydroxy(C₁-C₆)alkyl can be hydroxymethyl,1-hydroxyethyl, 2-hydroxyethyl, 1-hydroxypropyl, 2-hydroxypropyl,3-hydroxypropyl, 1-hydroxybutyl, 4-hydroxybutyl, 1-hydroxypentyl,5-hydroxypentyl, 1-hydroxyhexyl, or 6-hydroxyhexyl;(C₁-C₆)alkoxycarbonyl can be methoxycarbonyl, ethoxycarbonyl,propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, pentoxycarbonyl, orhexyloxycarbonyl; (C₁-C₆)alkylthio can be methylthio, ethylthio,propylthio, isopropylthio, butylthio, isobutylthio, pentylthio, orhexylthio; (C₂-C₆)alkanoyloxy can be acetoxy, propanoyloxy, butanoyloxy,isobutanoyloxy, pentanoyloxy, or hexanoyloxy.

“Alkynyl” refers to a cyclic, branched or straight chain groupcontaining only carbon and hydrogen, and unless otherwise mentionedtypically contains one to twelve carbon atoms, and contains one or moretriple bonds. Alkynyl groups may be unsubstituted or substituted. “Loweralkynyl” groups are those that contain one to six carbon atoms.

The term “amine” or “amino” refers to a group of the formula —NRR′,where R and R′ can be, independently, hydrogen or an alkyl, alkenyl,alkynyl, aryl, aralkyl, cycloalkyl, halogenated alkyl, acyl orheterocycloalkyl group. For example, an “alkylamino” or “alkylatedamino” refers to —NRR′, wherein at least one of R or R′ is an alkyl. An“acylamino” refers to —N(R)—C(O)—R (wherein R is a substituted groupsuch as alkyl or H). A suitable acylamino group is acetamido.

The term “aminoalkyl” refers to alkyl groups as defined above where atleast one hydrogen atom is replaced with an amino group (e.g, —CH₂—NH2).

“Aminocarbonyl” alone or in combination, means an amino substitutedcarbonyl (carbamoyl) radical, wherein the amino radical may optionallybe mono- or di-substituted, such as with alkyl, aryl, aralkyl,cycloalkyl, cycloalkylalkyl, alkanoyl, alkoxycarbonyl, aralkoxycarbonyland the like. An illustrative aminocarbonyl is —CONH₂. The term “amide”or “amido” is represented by the formula —C(O)NRR′, where R and R′independently can be a hydrogen, alkyl, alkenyl, alkynyl, aryl, aralkyl,cycloalkyl, halogenated alkyl, or heterocycloalkyl group.

An “analog” is a molecule that differs in chemical structure from aparent compound, for example a homolog (differing by an increment in thechemical structure or mass, such as a difference in the length of analkyl chain or the inclusion of one of more isotopes), a molecularfragment, a structure that differs by one or more functional groups, ora change in ionization. An analog is not necessarily synthesized fromthe parent compound. A derivative is a molecule derived from the basestructure.

An “animal” refers to living multi-cellular vertebrate organisms, acategory that includes, for example, mammals and birds. The term mammalincludes both human and non-human mammals. Similarly, the term “subject”includes both human and non-human subjects, including birds andnon-human mammals, such as non-human primates, companion animals (suchas dogs and cats), livestock (such as pigs, sheep, cows), as well asnon-domesticated animals, such as the big cats. The term subject appliesregardless of the stage in the organism's life-cycle. Thus, the termsubject applies to an organism in utero or in ovo, depending on theorganism (that is, whether the organism is a mammal or a bird, such as adomesticated or wild fowl).

The term “aralkyl” refers to an alkyl group wherein an aryl group issubstituted for a hydrogen of the alkyl group. An example of an aralkylgroup is a benzyl group.

“Aryl” refers to a monovalent unsaturated aromatic carbocyclic grouphaving a single ring (e.g., phenyl) or multiple condensed rings (e.g.,naphthyl or anthryl), which can optionally be unsubstituted orsubstituted. A “heteroaryl group,” is defined as an aromatic group thathas at least one heteroatom incorporated within the ring of the aromaticgroup. Examples of heteroatoms include, but are not limited to,nitrogen, oxygen, sulfur, and phosphorous. Heteroaryl includes, but isnot limited to, pyridinyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl,imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl, oxadiazolyl,thiophenyl, furanyl, quinolinyl, isoquinolinyl, benzimidazolyl,benzooxazolyl, quinoxalinyl, and the like. The aryl or heteroaryl groupcan be substituted with one or more groups including, but not limitedto, alkyl, alkynyl, alkenyl, aryl, halide, nitro, amino, ester, ketone,aldehyde, hydroxy, carboxylic acid, or alkoxy, or the aryl or heteroarylgroup can be unsubstituted.

“Aryloxy” or “heteroaryloxy” refers to a group of the formula —OAr,wherein Ar is an aryl group or a heteroaryl group, respectively.

The term “carboxylate” or “carboxyl” refers to the group —COO⁻ or —COOH.The carboxyl group can form a carboxylic acid. “Substituted carboxyl”refers to —COOR where R is alkyl, alkenyl, alkynyl, aryl, aralkyl,cycloalkyl, halogenated alkyl, or heterocycloalkyl group. For example, asubstituted carboxyl group could be a carboxylic acid ester or a saltthereof (e.g., a carboxylate).

“Carboxylalkyl” refers to an alkyl wherein one or more hydrogens of thealkyl is substituted with a carboxyl group (e.g., —RCOOH).

The term “co-administration” or “co-administering” refers toadministration of a compound disclosed herein with at least one othertherapeutic or diagnostic agent within the same general time period, anddoes not require administration at the same exact moment in time(although co-administration is inclusive of administering at the sameexact moment in time). Thus, co-administration may be on the same day oron different days, or in the same week or in different weeks.

The term “cycloalkyl” refers to a non-aromatic carbon-based ringcomposed of at least three carbon atoms. Examples of cycloalkyl groupsinclude, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, and the like. The term “heterocycloalkyl group” is acycloalkyl group as defined above where at least one of the carbon atomsof the ring is substituted with a heteroatom such as, but not limitedto, nitrogen, oxygen, sulfur, or phosphorous.

The term “ester” refers to a carboxyl group-containing moiety having thehydrogen replaced with, for example, a C₁₋₆alkyl group(“carboxylC₁₋₆alkyl” or “alkylester”), an aryl or aralkyl group(“arylester” or “aralkylester”) and so on. CO₂C₁₋₃alkyl groups arepreferred, such as for example, methylester (CO ₂Me), ethylester (CO₂Et)and propylester (CO₂Pr) and includes reverse esters thereof (e.g.—OCOMe, —OCOEt and —OCOPr).

The terms “halogenated alkyl” or “haloalkyl group” refer to an alkylgroup with one or more hydrogen atoms present on these groupssubstituted with a halogen (F, Cl, Br, I).

The term “hydroxyl” is represented by the formula —OH.

The term “hydroxyalkyl” refers to an alkyl group that has at least onehydrogen atom substituted with a hydroxyl group. The term “alkoxyalkylgroup” is defined as an alkyl group that has at least one hydrogen atomsubstituted with an alkoxy group described above.

“Inhibiting” refers to inhibiting the full development of a disease orcondition. “Inhibiting” also refers to any quantitative or qualitativereduction in biological activity or binding, relative to a control.

“N-heterocyclic” refers to mono or bicyclic rings or ring systems thatinclude at least one nitrogen hetero atom. The rings or ring systemsgenerally include 1 to 9 carbon atoms in addition to the heteroatom(s)and may be saturated, unsaturated or aromatic (includingpseudoaromatic). The term “pseudoaromatic” refers to a ring system whichis not strictly aromatic, but which is stabilized by means ofdelocalization of electrons and behaves in a similar manner to aromaticrings. Aromatic includes pseudoaromatic ring systems, such as pyrrolylrings.

Examples of 5-membered monocyclic N-heterocycles include pyrrolyl,H-pyrrolyl, pyrrolinyl, pyrrolidinyl, oxazolyl, oxadiazolyl, (including1,2,3 and 1,2,4 oxadiazolyls) isoxazolyl, furazanyl, thiazolyl,isothiazolyl, pyrazolyl, pyrazolinyl, pyrazolidinyl, imidazolyl,imidazolinyl, triazolyl (including 1,2,3 and 1,3,4 triazolyls),tetrazolyl, thiadiazolyl (including 1,2,3 and 1,3,4 thiadiazolyls), anddithiazolyl. Examples of 6-membered monocyclic N-heterocycles includepyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, piperidinyl, morpholinyl,thiomorpholinyl, piperazinyl, and triazinyl. The N-heterocycles may beoptionally substituted with a broad range of substituents, andpreferably with C₁₋₆alkyl, C₁₋₆alkoxy, C₂₋₆alkenyl, C₂₋₆alkynyl, halo,hydroxy, mercapto, trifluoromethyl, amino, cyano or mono ordi(C₁₋₆alkyl)amino. The N-heterocyclic group may be fused to acarbocyclic ring such as phenyl, naphthyl, indenyl, azulenyl, fluorenyl,and anthracenyl.

Examples of 8, 9 and 10-membered bicyclic heterocycles include 1Hthieno[2,3-c]pyrazolyl, indolyl, isoindolyl, benzoxazolyl,benzothiazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazolyl,indazolyl, isoquinolinyl, quinolinyl, quinoxalinyl, purinyl, cinnolinyl,phthalazinyl, quinazolinyl, quinoxalinyl, benzotriazinyl, and the like.These heterocycles may be optionally substituted, for example withC₁₋₆alkyl, C₁₋₆alkoxy, C₂₋₆alkenyl, C₂₋₆alkynyl, halo, hydroxy,mercapto, trifluoromethyl, amino, cyano or mono or di(C₁₋₆alkyl)aminoUnless otherwise defined optionally substituted N-heterocyclics includespyridinium salts and the N-oxide form of suitable ring nitrogens.

The term “subject” includes both human and non-human subjects, includingbirds and non-human mammals, such as non-human primates, companionanimals (such as dogs and cats), livestock (such as pigs, sheep, cows),as well as non-domesticated animals, such as the big cats. The termsubject applies regardless of the stage in the organism's life-cycle.Thus, the term subject applies to an organism in utero or in ovo,depending on the organism (that is, whether the organism is a mammal ora bird, such as a domesticated or wild fowl).

“Substituted” or “substitution” refers to replacement of a hydrogen atomof a molecule or an R-group with one or more additional R-groups. Unlessotherwise defined, the term “optionally-substituted” or “optionalsubstituent” as used herein refers to a group which may or may not befurther substituted with 1, 2, 3, 4 or more groups, preferably 1, 2 or3, more preferably 1 or 2 groups. The substituents may be selected, forexample, from C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₈cycloalkyl,hydroxyl, oxo, C₁₋₆alkoxy, aryloxy, C₁₋₆alkoxyaryl, halo, C₁₋₆alkylhalo(such as CF₃ and CHF₂), C₁₋₆alkoxyhalo (such as OCF₃ and OCHF₂),carboxyl, esters, cyano, nitro, amino, substituted amino, disubstitutedamino, acyl, ketones, amides, aminoacyl, substituted amides,disubstituted amides, thiol, alkylthio, thioxo, sulfates, sulfonates,sulfinyl, substituted sulfinyl, sulfonyl, substituted sulfonyl,sulfonylamides, substituted sulfonamides, disubstituted sulfonamides,aryl, arC₁₋₆alkyl, heterocyclyl and heteroaryl wherein each alkyl,alkenyl, alkynyl, cycloalkyl, aryl and heterocyclyl and groupscontaining them may be further optionally substituted. Optionalsubstituents in the case N-heterocycles may also include but are notlimited to C₁₋₆alkyl i.e. N—C₁₋₃alkyl.

“Sulfinyl” refers to the group —S(═O)H.

The term “substituted sulfinyl” or “sulfoxide” refers to a sulfinylgroup having the hydrogen replaced with, for example a C₁₋₆alkyl group(“C₁₋₆alkylsulfinyl” or “C₁₋₆alkylsulfoxide”), an aryl (“arylsulfinyl”),an aralkyl (“aralkyl sulfinyl”) and so on. C₁₋₃alkylsulfinyl groups arepreferred, such as for example, —SOmethyl, —SOethyl and —SOpropyl.

The term “sulfonyl” refers to the group —SO₂H.

The term “substituted sulfonyl” refers to a sulfonyl group having thehydrogen replaced with, for example a C₁₋₆alkyl group(“sulfonylC₁₋₆alkyl”), an aryl (“arylsulfonyl”), an aralkyl(“aralkylsulfonyl”) and so on. SulfonylC₁₋₃alkyl groups are preferred,such as for example, —SO₂Me, —SO₂Et and —SO₂Pr.

The term “sulfonylamido” or “sulfonamide” refers to the group —SO₂NH2.

A “therapeutically effective amount” refers to a quantity of a specifiedagent sufficient to achieve a desired effect in a subject being treatedwith that agent. Ideally, a therapeutically effective amount of an agentis an amount sufficient to inhibit or treat the disease or conditionwithout causing a substantial toxic effect in the subject. Thetherapeutically effective amount of an agent will be dependent on thesubject being treated, the severity of the affliction, and the manner ofadministration of the therapeutic composition.

“Treatment” refers to a therapeutic intervention that ameliorates a signor symptom of a disease or pathological condition after it has begun todevelop, or administering a compound or composition to a subject whodoes not exhibit signs of a disease or exhibits only early signs for thepurpose of decreasing the risk of developing a pathology or condition,or diminishing the severity of a pathology or condition. As used herein,the term “ameliorating,” with reference to a disease or pathologicalcondition, refers to any observable beneficial effect of the treatment.The beneficial effect can be evidenced, for example, by a delayed onsetof clinical symptoms of the disease in a susceptible subject, areduction in severity of some or all clinical symptoms of the disease, aslower progression of the disease, an improvement in the overall healthor well-being of the subject, or by other parameters well known in theart that are specific to the particular disease. The phrase “treating adisease” refers to inhibiting the full development of a disease, forexample, in a subject who is at risk for a disease such as diabetes.“Preventing” a disease or condition refers to prophylactic administeringa composition to a subject who does not exhibit signs of a disease orexhibits only early signs for the purpose of decreasing the risk ofdeveloping a pathology or condition, or diminishing the severity of apathology or condition.

“Pharmaceutical compositions” are compositions that include an amount(for example, a unit dosage) of one or more of the disclosed compoundstogether with one or more non-toxic pharmaceutically acceptableadditives, including carriers, diluents, and/or adjuvants, andoptionally other biologically active ingredients. Such pharmaceuticalcompositions can be prepared by standard pharmaceutical formulationtechniques such as those disclosed in Remington's PharmaceuticalSciences, Mack Publishing Co., Easton, Pa. (19th Edition).

The terms “pharmaceutically acceptable salt or ester” refers to salts oresters prepared by conventional means that include salts, e.g., ofinorganic and organic acids, including but not limited to hydrochloricacid, hydrobromic acid, sulfuric acid, phosphoric acid, methanesulfonicacid, ethanesulfonic acid, malic acid, acetic acid, oxalic acid,tartaric acid, citric acid, lactic acid, fumaric acid, succinic acid,maleic acid, salicylic acid, benzoic acid, phenylacetic acid, mandelicacid and the like. “Pharmaceutically acceptable salts” of the presentlydisclosed compounds also include those formed from cations such assodium, potassium, aluminum, calcium, lithium, magnesium, zinc, and frombases such as ammonia, ethylenediamine, N-methyl-glutamine, lysine,arginine, ornithine, choline, N,N′-dibenzylethylenediamine,chloroprocaine, diethanolamine, procaine, N-benzylphenethylamine,diethylamine, piperazine, tris(hydroxymethyl)aminomethane, andtetramethylammonium hydroxide. These salts may be prepared by standardprocedures, for example by reacting the free acid with a suitableorganic or inorganic base. Any chemical compound recited in thisspecification may alternatively be administered as a pharmaceuticallyacceptable salt thereof. “Pharmaceutically acceptable salts” are alsoinclusive of the free acid, base, and zwitterionic forms. Descriptionsof suitable pharmaceutically acceptable salts can be found in Handbookof Pharmaceutical Salts, Properties, Selection and Use, Wiley VCH(2002). When compounds disclosed herein include an acidic function suchas a carboxy group, then suitable pharmaceutically acceptable cationpairs for the carboxy group are well known to those skilled in the artand include alkaline, alkaline earth, ammonium, quaternary ammoniumcations and the like. Such salts are known to those of skill in the art.For additional examples of “pharmacologically acceptable salts,” seeBerge et al., J. Pharm. Sci. 66:1 (1977).

“Pharmaceutically acceptable esters” includes those derived fromcompounds described herein that are modified to include a carboxylgroup. An in vivo hydrolysable ester is an ester, which is hydrolysed inthe human or animal body to produce the parent acid or alcohol.Representative esters thus include carboxylic acid esters in which thenon-carbonyl moiety of the carboxylic acid portion of the ester groupingis selected from straight or branched chain alkyl (for example, methyl,n-propyl, t-butyl, or n-butyl), cycloalkyl, alkoxyalkyl (for example,methoxymethyl), aralkyl (for example benzyl), aryloxyalkyl (for example,phenoxymethyl), aryl (for example, phenyl, optionally substituted by,for example, halogen, C.sub.1-4 alkyl, or C.sub.1-4 alkoxy) or amino);sulphonate esters, such as alkyl- or aralkylsulphonyl (for example,methanesulphonyl); or amino acid esters (for example, L-valyl orL-isoleucyl). A “pharmaceutically acceptable ester” also includesinorganic esters such as mono-, di-, or tri-phosphate esters. In suchesters, unless otherwise specified, any alkyl moiety presentadvantageously contains from 1 to 18 carbon atoms, particularly from 1to 6 carbon atoms, more particularly from 1 to 4 carbon atoms. Anycycloalkyl moiety present in such esters advantageously contains from 3to 6 carbon atoms. Any aryl moiety present in such esters advantageouslycomprises a phenyl group, optionally substituted as shown in thedefinition of carbocycylyl above. Pharmaceutically acceptable estersthus include C₁-C₂₂ fatty acid esters, such as acetyl, t-butyl or longchain straight or branched unsaturated or omega-6 monounsaturated fattyacids such as palmoyl, stearoyl and the like. Alternative aryl orheteroaryl esters include benzoyl, pyridylmethyloyl and the like any ofwhich may be substituted, as defined in carbocyclyl above. Additionalpharmaceutically acceptable esters include aliphatic L-amino acid esterssuch as leucyl, isoleucyl and especially valyl.

For therapeutic use, salts of the compounds are those wherein thecounter-ion is pharmaceutically acceptable. However, salts of acids andbases which are non-pharmaceutically acceptable may also find use, forexample, in the preparation or purification of a pharmaceuticallyacceptable compound.

The pharmaceutically acceptable acid and base addition salts asmentioned hereinabove are meant to comprise the therapeutically activenon-toxic acid and base addition salt forms which the compounds are ableto form. The pharmaceutically acceptable acid addition salts canconveniently be obtained by treating the base form with such appropriateacid. Appropriate acids comprise, for example, inorganic acids such ashydrohalic acids, e.g. hydrochloric or hydrobromic acid, sulfuric,nitric, phosphoric and the like acids; or organic acids such as, forexample, acetic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic (i.e.ethanedioic), malonic, succinic (i.e. butanedioic acid), maleic,fumaric, malic (i.e. hydroxybutanedioic acid), tartaric, citric,methanesulfonic, ethanesulfonic, benzenesulfonic, p-toluenesulfonic,cyclamic, salicylic, p-aminosalicylic, pamoic and the like acids.Conversely said salt forms can be converted by treatment with anappropriate base into the free base form.

The compounds containing an acidic proton may also be converted intotheir non-toxic metal or amine addition salt forms by treatment withappropriate organic and inorganic bases. Appropriate base salt formscomprise, for example, the ammonium salts, the alkali and alkaline earthmetal salts, e.g. the lithium, sodium, potassium, magnesium, calciumsalts and the like, salts with organic bases, e.g. the benzathine,N-methyl-D-glucamine, hydrabamine salts, and salts with amino acids suchas, for example, arginine, lysine and the like.

The term “addition salt” as used hereinabove also comprises the solvateswhich the compounds described herein are able to form. Such solvates arefor example hydrates, alcoholates and the like.

The term “quaternary amine” as used hereinbefore defines the quaternaryammonium salts which the compounds are able to form by reaction betweena basic nitrogen of a compound and an appropriate quaternizing agent,such as, for example, an optionally substituted alkylhalide, arylhalideor arylalkylhalide, e.g. methyliodide or benzyliodide. Other reactantswith good leaving groups may also be used, such as alkyltrifluoromethanesulfonates, alkyl methanesulfonates, and alkylp-toluenesulfonates. A quaternary amine has a positively chargednitrogen. Pharmaceutically acceptable counterions include chloro, bromo,iodo, trifluoroacetate and acetate. The counterion of choice can beintroduced using ion exchange resins.

Prodrugs of the disclosed compounds also are contemplated herein. Aprodrug is an active or inactive compound that is modified chemicallythrough in vivo physiological action, such as hydrolysis, metabolism andthe like, into an active compound following administration of theprodrug to a subject. The term “prodrug” as used throughout this textmeans the pharmacologically acceptable derivatives such as esters,amides and phosphates, such that the resulting in vivo biotransformationproduct of the derivative is the active drug as defined in the compoundsdescribed herein. Prodrugs preferably have excellent aqueous solubility,increased bioavailability and are readily metabolized into the activeinhibitors in vivo. Prodrugs of a compounds described herein may beprepared by modifying functional groups present in the compound in sucha way that the modifications are cleaved, either by routine manipulationor in vivo, to the parent compound. The suitability and techniquesinvolved in making and using prodrugs are well known by those skilled inthe art. F or a general discussion of prodrugs involving esters seeSvensson and Tunek, Drug Metabolism Reviews 165 (1988) and Bundgaard,Design of Prodrugs, Elsevier (1985).

The term “prodrug” also is intended to include any covalently bondedcarriers that release an active parent drug of the present invention invivo when the prodrug is administered to a subject. Since prodrugs oftenhave enhanced properties relative to the active agent pharmaceutical,such as, solubility and bioavailability, the compounds disclosed hereincan be delivered in prodrug form. Thus, also contemplated are prodrugsof the presently disclosed compounds, methods of delivering prodrugs andcompositions containing such prodrugs. Prodrugs of the disclosedcompounds typically are prepared by modifying one or more functionalgroups present in the compound in such a way that the modifications arecleaved, either in routine manipulation or in vivo, to yield the parentcompound. Prodrugs include compounds having a phosphonate and/or aminogroup functionalized with any group that is cleaved in vivo to yield thecorresponding amino and/or phosphonate group, respectively. Examples ofprodrugs include, without limitation, compounds having an acylated aminogroup and/or a phosphonate ester or phosphonate amide group. Inparticular examples, a prodrug is a lower alkyl phosphonate ester, suchas an isopropyl phosphonate ester.

Protected derivatives of the disclosed compounds also are contemplated.A variety of suitable protecting groups for use with the disclosedcompounds are disclosed in Greene and Wuts, Protective Groups in OrganicSynthesis; 3rd Ed.; John Wiley & Sons, New York, 1999.

In general, protecting groups are removed under conditions that will notaffect the remaining portion of the molecule. These methods are wellknown in the art and include acid hydrolysis, hydrogenolysis and thelike. One preferred method involves the removal of an ester, such ascleavage of a phosphonate ester using Lewis acidic conditions, such asin TMS-Br mediated ester cleavage to yield the free phosphonate. Asecond preferred method involves removal of a protecting group, such asremoval of a benzyl group by hydrogenolysis utilizing palladium oncarbon in a suitable solvent system such as an alcohol, acetic acid, andthe like or mixtures thereof. A t-butoxy-based group, including t-butoxycarbonyl protecting groups can be removed utilizing an inorganic ororganic acid, such as HCl or trifluoroacetic acid, in a suitable solventsystem, such as water, dioxane and/or methylene chloride. Anotherexemplary protecting group, suitable for protecting amino and hydroxyfunctions amino is trityl. Other conventional protecting groups areknown and suitable protecting groups can be selected by those of skillin the art in consultation with Greene and Wuts, Protective Groups inOrganic Synthesis; 3rd Ed.; John Wiley & Sons, New York, 1999. When anamine is deprotected, the resulting salt can readily be neutralized toyield the free amine. Similarly, when an acid moiety, such as aphosphonic acid moiety is unveiled, the compound may be isolated as theacid compound or as a salt thereof.

The usefulness of diaryl enone compounds is impeded by limited watersolubility. This drawback is especially relevant to treatment of lungdisease, since inhalation of a nebulized formulation is the preferredmethod for delivery of therapeutic agents to the lung. Delivery of adrug by inhalation allows deposition of the drug into different sectionsof the respiratory tract, including the throat, trachea, bronchi andalveoli. Generally, the smaller the size of the inhaled particle thelonger it will remain suspended in air and the farther down therespiratory tract the inhaled drug can be delivered. The desiredproperties of a liquid for nebulization generally include: 1) lowviscosity; 2) sterile medium; 3) low surface tension; 4) stabilitytoward the mechanism of nebulization; 5) moderate pH (about 4-10); 6)ability to form droplets; 7) absence of irritating preservatives andstabilizing agents; and 8) suitable tonicity. A wide variety ofnebulizers differing in mode of operation are available. These includeultrasonic, vibrating membrane, vibrating mesh, vibrating plate,vibrating cone, micropump, and jet nebulizers along with others. Thevibrating mesh, vibrating cone or vibrating plate nebulizers are ofparticular interest since they do not require the use of an aircompressor for delivery, have a minimal residual volume in the reservoirafter delivery of a unit dose, and can be used to deliver low volumes ofinhalable solutions. The principle advantages of nebulizers over othermethods of pulmonary installation are that patient cooperation is notrequired and it is easier to deliver high doses of medication.

As many thiol-containing compounds are highly hydrophilic, they may formwater-soluble adducts with diaryl enone compounds. The resultingwater-soluble compounds could then not only be incorporated intonebulizable formulations for delivery to the lung by inhalation but mayfreely enter cells, where the diaryl enone component could exerttherapeutic effects either by forming adducts with cysteine residues,accompanied by displacement of the original thiol residue, or by othermeans. Based on these considerations, disclosed herein are novel thiolderivatives of specific, novel, diaryl enones. Also disclosed areformulations of these compounds suitable for pulmonary delivery andtheir use for treating pulmonary disease.

Disclosed herein in certain embodiments are novel diaryl enone compoundsthat possess anti-inflammatory, antioxidant, and other therapeuticproperties. Also described are nebulized aerosol or dry powderformulations of these compounds that are suitable for delivery to thepulmonary system by inhalation. Further described are uses of thesecompounds and formulations for treatment of various pulmonary diseases.The therapeutically useful compounds may be rendered water-soluble, forexample, though formation of suitable thiol derivatives.

In one aspect, the novel compounds may be produced by chemicallycombining a diaryl enone compound with a thiol that renders the finalcompound water-soluble. Such water-soluble compounds can readily entercells, where the synthetically added thiols may be displaced byintracellular thiols such as the cysteine residues in various proteins.The aryl groups are composed of unique di- or tri-nitrogen containingmoieties, in which the inductive effects of the nitrogen atoms induce apartially positive charge on the carbon atoms. Because of the low-lyingunoccupied π-molecular orbitals in these nitrogen-containing compounds,and their derivatives, these compounds demonstrate uniquephysico-chemical properties and the ability to act as a bridging ligand.

Compounds

Disclosed herein are compounds, or a pharmaceutically acceptable salt orester thereof, comprising an adduct of a hydrophilic thiol and an enonethat comprises at least two N-heterocycles.

For example, one embodiment is a compound, or a pharmaceuticallyacceptable salt or ester thereof, having a structure of:

X¹-L-X²

wherein L is a linking moiety comprising an enone; andX¹ and X² are each independently an optionally-substitutedN-heterocycle.

L, for example, may be an alkyl-1,4-diene-3-one such aspenta-1,4-dien-3-one, or an alkyl-1,5-thiol-3-one such aspenta-1,5-thiol-3-one, wherein each thiol is optionally substituted.Other substituted alkyl dienes with each double bond adjacent to aketone are equally suitable, as are aryl ketones with thiol groupspositioned between tow carbons from the ketone.

In certain embodiments, X¹ and X² are the same, and are each, forexample, pyrazinyl or pyrimidinyl.

In a further embodiment, there is disclosed is a compound, or apharmaceutically acceptable salt or ester thereof, having a structureof:

wherein

represents a single bond or a double bond;A is CH if

is a double bond, or CH(S—R⁵) if

is a single bond, wherein R⁵ is a peptide, amino acid, amino acidderivative, optionally-substituted alkyl, optionally-substitutedalkenyl, optionally-substituted alkynyl, optionally-substitutedcycloalkyl, or optionally-substituted cycloalkenyl; andX¹ and X² are each independently an optionally-substitutedN-heterocycle; or

wherein

represents a single bond or a double bond;A is CH if

is a double bond, or CH(S—R⁵) if

is a single bond, wherein R⁵ is a peptide, amino acid, amino acidderivative, optionally-substituted alkyl, optionally-substitutedalkenyl, optionally-substituted alkynyl, optionally-substitutedcycloalkyl, or optionally-substituted cycloalkenyl;X¹ and X² are each independently an optionally-substitutedN-heterocycle; andR¹, R², and R³ are each independently C or N; or

wherein

represents a single bond or a double bond;A is CH if

is a double bond, or CH(S—R⁵) if

is a single bond, wherein R⁵ is a peptide, amino acid, amino acidderivative, optionally-substituted alkyl, optionally-substitutedalkenyl, optionally-substituted alkynyl, optionally-substitutedcycloalkyl, or optionally-substituted cycloalkenyl;X¹ and X² are each independently an optionally-substitutedN-heterocycle; and

R¹ is C or N; or

wherein

represents a single bond or a double bond;A is CH if

is a double bond, or CH(S—R⁵) if

is a single bond, wherein R⁵ is a peptide, amino acid, amino acidderivative, optionally-substituted alkyl, optionally-substitutedalkenyl, optionally-substituted alkynyl, optionally-substitutedcycloalkyl, or optionally-substituted cycloalkenyl;R¹ and R² are each independently C or N; andX¹ and X² are each independently an optionally-substitutedN-heterocycle.

In the compound described above, X¹ may have a structure of:

and X² has a structure of:

wherein Z¹, Z², and Z³ are each independently C or N, provided that atleast one of Z¹, Z², or Z³ is N; andY¹, Y², Y³, Y⁴ and Y⁵ are each independently H, optionally-substitutedalkyl, optionally-substituted amino, hydroxyl, optionally-substitutedalkoxy, optionally-substituted thiol, acyl, or halogen.

In certain embodiments, the compound has a structure of:

In certain embodiments, the compound has a structure of:

In certain embodiments, the compound has a structure of:

In certain embodiments, the compound has a structure of:

In certain embodiments, X¹ and X² are each optionally-substitutedpyrazinyl or optionally-substituted pyrimidinyl.

In certain embodiments, R⁵ is an acylamino-substituted carboxylalkyl, asulfonate-substituted alkyl, or an acylamino-substituted amido. Incertain embodiments, R⁵ is a sugar derivative.

In certain embodiments, the —S—R⁵ moiety is a derivative ofN-acetylcysteine, 2-mercaptoethane sulfonate, or glutathione.

Illustrative compounds are shown below:

Thiol adduct of PB137, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB141 (NAC adduct of PB137)

PB142 (mercaptoethane sulfonate adduct of PB137)

PB143 (glutathione adduct to PB137)

PB151

Thiol adduct of PB151, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB157

PB158

PB159

PB161

Thiol adduct of PB161, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB167

PB168

PB169 (glutathione adduct of PB161)

PB171

Thiol adduct of PB171, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB177 (NAC adduct of PB171)

PB178 (mercaptoethanesulfonate adduct of PB171)

PB179 (glutathione adduct of PB171)

PB200

Thiol adducts of PB200, wherein —SR may be derived fromN-acetylcysteine, 2-mercaptoethane sulfonate, glutathione, or anothersuitable thiol compound

PB201 (NAC adduct of PB200)

PB202 (mercaptoethanesulfonate adduct of PB200)

PB203 (glutathione adduct of PB200)

PB204

Thiol adduct of PB204, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB205 (NAC adduct of PB204)

PB206 (mercaptoethanesulfonate adduct of PB204)

PB207 (glutathione adduct of PB204)

PB208

Thiol adduct of PB208, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB209 (NAC adduct of PB208)

PB210 (mercaptoethanesulfonate adduct of PB208)

PB211 (glutathione adduct of PB208)

PB212

-   Thiol adduct of PB212, wherein —SR may be derived from    N-acetylcysteine, 2-mercaptoethane sulfonate, glutathione, or    another suitable thiol compound

PB213 (NAC adduct of PB212)

PB214 (mercaptoethanesulfonate adduct of PB212)

PB215 (glutathione adduct of PB212)

PB216

Thiol adduct of PB216, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB217 (NAC adduct of PB216)

PB218 (mercaptoethanesulfonate adduct of PB216)

PB219 (glutathione adduct of PB216)

PB220

-   Thiol adduct of PB220, wherein —SR may be derived from    N-acetylcysteine, 2-mercaptoethane sulfonate, glutathione, or    another suitable thiol compound

PB221 (NAC adduct of PB220)

PB222 (mercaptoethanesulfonate adduct of PB220)

PB223 (glutathione adduct of PB220)

PB224

Thiol adduct of PB224, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB225 (NAC adduct of PB224)

PB226 (mercaptoethanesulfonate adduct of PB224)

PB227 (glutathione adduct of PB224)

PB228

Thiol adduct of PB228, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB229 (NAC adduct of PB228)

PB230 (mercaptoethanesulfonate adduct of PB228)

PB231 (glutathione adduct of PB228)

PB232

Thiol adduct of PB232, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB233 (NAC adduct of PB232)

PB234 (mercaptoethanesulfonate adduct of PB232)

PB235 (glutathione adduct of PB232)

PB236

Thiol adduct of PB236, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB237 (NAC adduct of PB236)

PB238 (mercaptoethanesulfonate adduct of PB236)

PB239 (glutathione adduct of PB236)

PB240

Thiol adduct of PB240, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB241 (NAC adduct of PB240)

PB242 (mercaptoethanesulfonate adduct of PB240)

PB243 (glutathione adduct of PB240)

PB244

Thiol adduct of PB244, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB245 (NAC adduct of PB244)

PB246 (mercaptoethanesulfonate adduct of PB244)

PB247 (glutathione adduct of PB244)

PB248

Thiol adduct of PB248, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB249 (NAC adduct of PB248)

PB250 (mercaptoethanesulfonate adduct of PB248)

PB251 (glutathione adduct of PB248)

PB252

Thiol adduct of PB252, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB253 (NAC adduct of PB252)

PB254 (mercaptoethanesulfonate adduct of PB252)

PB255 (glutathione adduct of PB252)

PB256

Thiol adduct of PB256, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB257 (NAC adduct of PB256)

PB258 (mercaptoethanesulfonate adduct of PB256)

PB259 (glutathione adduct of PB256)

PB260

Thiol adduct of PB260, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB261 (NAC adduct of PB260)

PB262 (mercaptoethanesulfonate adduct of PB260)

PB263 (glutathione adduct of PB260)

PB264

-   Thiol adduct of PB264, wherein —SR may be derived from    N-acetylcysteine, 2-mercaptoethane sulfonate, glutathione, or    another suitable thiol compound

PB265 (NAC adduct of PB264)

PB266 (mercaptoethanesulfonate adduct of PB264)

PB267 (glutathione adduct of PB264)

PB268

Thiol adduct of PB268, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB269 (NAC adduct of PB268)

PB270 (mercaptoethanesulfonate adduct of PB268)

PB271 (glutathione adduct of PB268)

PB272

Thiol adduct of PB272, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB273 (NAC adduct PB272)

PB274 (mercaptoethanesulfonate adduct of PB272)

PB275 (glutathione adduct of PB272)

PB276

Thiol adduct of PB276, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB277 (NAC adduct of PB276)

PB278 (mercaptoethanesulfonate adduct of PB276)

PB279 (glutathione adduct of PB276)

PB280

Thiol adduct of PB280, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB281 (NAC adduct of PB280)

PB282 (mercaptoethanesulfonate adduct of PB280)

PB283 (glutathione adduct of PB280)

PB284

Thiol adduct of PB284, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB285 (NAC adduct of PB284)

PB286 (mercaptoethanesulfonate adduct of PB284)

PB287 (glutathione adduct of PB284)

PB288

Thiol adduct of PB288, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB289 (NAC adduct of PB288)

PB290 (mercaptoethanesulfonate adduct of PB288)

PB291 (glutathione adduct of PB288)

PB292

Thiol adduct of PB292, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB293 (NAC adduct of PB292)

PB294 (mercaptoethanesulfonate adduct of PB292)

PB295 (glutathione adduct of PB292)

PB296

Thiol adduct of PB296, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB297 (NAC adduct of PB296)

PB298 (mercaptoethanesulfonate adduct of PB296)

PB299 (glutathione adduct of PB296)

PB300

Thiol adduct of PB300, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB301 (NAC adduct of PB300)

PB302 (mercaptoethanesulfonate adduct of PB300)

PB303 (glutathione adduct of PB300)

PB304

Thiol adduct of PB304, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB305 (NAC adduct of PB304)

PB306 (mercaptoethanesulfonate adduct of PB304)

PB307 (glutathione adduct of PB304)

PB308

Thiol adduct of PB308, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB309 (NAC adduct of PB308)

PB310 (mercaptoethanesulfonate adduct of PB308)

PB311 (glutathione adduct of PB308)

PB312

Thiol adduct of PB312, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB313 (NAC adduct of PB312)

PB314 (mercaptoethanesulfonate adduct of PB312)

PB315 (glutathione adduct of PB312)

PB316

Thiol adduct of PB316, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB317 (NAC adduct of PB316)

PB318 (mercaptoethanesulfonate adduct of PB316)

PB319 (glutathione adduct of PB316)

PB320

Thiol adduct of PB320, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB321 (NAC adduct of PB320)

PB322 (mercaptoethanesulfonate adduct of PB320)

PB323 (glutathione adduct of PB320)

PB324

Thiol adduct of PB324, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB325 (NAC adduct of PB324)

PB326 (mercaptoethanesulfonate adduct of PB324)

PB327 (glutathione adduct of PB324)

PB328

Thiol adduct of PB328, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB329 (NAC adduct of PB328)

PB330 (mercaptoethanesulfonate adduct of PB328)

PB331 (glutathione adduct of PB328)

PB332

Thiol adduct of PB332, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB333 (NAC adduct of PB332)

PB334 (mercaptoethanesulfonate adduct of PB332)

PB335 (glutathione adduct of PB332)

PB336

Thiol adduct of PB336, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB337 (NAC adduct of PB336)

PB338 (mercaptoethanesulfonate adduct of PB336)

PB339 (glutathione adduct of PB336)

PB340

Thiol adduct of PB340, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB341 (NAC adduct of PB340)

PB342 (mercaptoethanesulfonate adduct of PB340)

PB343 (glutathione adduct of PB340)

PB344

Thiol adduct of PB344, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB345 (NAC adduct of PB344)

PB346 (mercaptoethanesulfonate adduct of PB344)

PB347 (glutathione adduct of PB344)

PB348

Thiol adduct of PB348, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB349 (NAC adduct of PB348)

PB350 (mercaptoethanesulfonate adduct of PB348)

PB351 (glutathione adduct of PB348)

PB352

Thiol adduct of PB352, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB353 (NAC adduct of PB352)

PB354 (mercaptoethanesulfonate adduct of PB352)

PB355 (glutathione adduct of PB352)

PB356

Thiol adduct of PB356, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB357 (NAC adduct of PB356)

PB358 (mercaptoethanesulfonate adduct of PB356)

PB359 (glutathione adduct of PB356)

PB360

Thiol adduct of PB360, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB361 (NAC adduct of PB360)

PB362 (mercaptoethanesulfonate adduct of PB360)

PB363 (glutathione adduct of PB360)

PB364

Thiol adduct of PB364, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB365 (NAC adduct of PB364)

PB366 (mercaptoethanesulfonate adduct of PB364)

PB367 (glutathione adduct of PB364)

PB368

Thiol adduct of PB368, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB369 (NAC adduct of PB368)

PB370 (mercaptoethanesulfonate adduct of PB368)

PB371 (glutathione adduct of PB368)

PB372

Thiol adduct of PB372, wherein —SR may be derived from N-acetylcysteine,2-mercaptoethane sulfonate, glutathione, or another suitable thiolcompound

PB373 (NAC adduct of PB372)

PB374 (mercaptoethanesulfonate adduct of PB372)

PB375 (glutathione adduct of PB372)

Pharmaceutical Compositions and Methods of Use

In certain embodiments, the compounds described herein may be useful fortreating pulmonary diseases, such as lung diseases. The lung is the siteof a wide variety of diseases and pathological conditions. Illustrativepulmonary diseases include pulmonary fibrosis, chronic obstructivepulmonary disease (COPD), asthma, cystic fibrosis, acute lung injury(ALI), acute respiratory distress syndrome, pulmonary hypertension, lungcancer and pulmonary manifestations of cystic fibrosis.

In certain embodiments, the compounds disclosed herein are antioxidants.For example, the compounds may oxidize radicals (e.g., oxidants,cations, etc.) that are deleterious to lung tissue.

In certain embodiments, the compounds disclosed herein may be useful fortreating ischemia-reperfusion injury.

In certain embodiments, the compounds disclosed herein may inhibit NF-κBactivity.

In certain embodiments, the compounds disclosed herein may inhibit lungfibroblast proliferation.

In certain embodiments, the compounds disclosed herein may inhibitmyofibroblast differentiation.

In certain embodiments, the compounds described herein may be useful inameliorating or preventing acute and chronic rejection of transplantedorgans, particularly lungs.

Also disclosed herein are methods for efficiently delivering thecompounds directly to the lung via formulations capable of producingeither nebulized aerosols or dry powders suitable for inhalation.

Another aspect of the disclosure includes pharmaceutical compositionsprepared for administration to a subject and which include atherapeutically effective amount of one or more of the compoundsdisclosed herein. The therapeutically effective amount of a disclosedcompound will depend on the route of administration, the species ofsubject and the physical characteristics of the subject being treated.Specific factors that can be taken into account include disease severityand stage, weight, diet and concurrent medications. The relationship ofthese factors to determining a therapeutically effective amount of thedisclosed compounds is understood by those of skill in the art.

Pharmaceutical compositions for administration to a subject can includeat least one further pharmaceutically acceptable additive such ascarriers, thickeners, diluents, buffers, preservatives, surface-activeagents and the like in addition to the molecule of choice.Pharmaceutical compositions can also include one or more additionalactive ingredients such as antimicrobial agents, anti-inflammatoryagents, anesthetics, and the like. The pharmaceutically acceptablecarriers useful for these formulations are conventional. Remington'sPharmaceutical Sciences, by E. W. Martin, Mack Publishing Co., Easton,Pa., 19th Edition (1995), describes compositions and formulationssuitable for pharmaceutical delivery of the compounds herein disclosed.

In general, the nature of the carrier will depend on the particular modeof administration being employed. For instance, parenteral formulationsusually contain injectable fluids that include pharmaceutically andphysiologically acceptable fluids such as water, physiological saline,balanced salt solutions, aqueous dextrose, glycerol or the like as avehicle. For solid compositions (for example, powder, pill, tablet, orcapsule forms), conventional non-toxic solid carriers can include, forexample, pharmaceutical grades of mannitol, lactose, starch, ormagnesium stearate. In addition to biologically-neutral carriers,pharmaceutical compositions to be administered can contain minor amountsof non-toxic auxiliary substances, such as wetting or emulsifyingagents, preservatives, and pH buffering agents and the like, for examplesodium acetate or sorbitan monolaurate.

Pharmaceutical compositions disclosed herein include those formed frompharmaceutically acceptable salts and/or solvates of the disclosedcompounds. Pharmaceutically acceptable salts include those derived frompharmaceutically acceptable inorganic or organic bases and acids.Particular disclosed compounds possess at least one basic group that canform acid-base salts with acids. Examples of basic groups include, butare not limited to, amino and imino groups. Examples of inorganic acidsthat can form salts with such basic groups include, but are not limitedto, mineral acids such as hydrochloric acid, hydrobromic acid, sulfuricacid or phosphoric acid. Basic groups also can form salts with organiccarboxylic acids, sulfonic acids, sulfo acids or phospho acids orN-substituted sulfamic acid, for example acetic acid, propionic acid,glycolic acid, succinic acid, maleic acid, hydroxymaleic acid,methylmaleic acid, fumaric acid, malic acid, tartaric acid, gluconicacid, glucaric acid, glucuronic acid, citric acid, benzoic acid,cinnamic acid, mandelic acid, salicylic acid, 4-aminosalicylic acid,2-phenoxybenzoic acid, 2-acetoxybenzoic acid, embonic acid, nicotinicacid or isonicotinic acid, and, in addition, with amino acids, forexample with α-amino acids, and also with methanesulfonic acid,ethanesulfonic acid, 2-hydroxymethanesulfonic acid,ethane-1,2-disulfonic acid, benzenedisulfonic acid,4-methylbenzenesulfonic acid, naphthalene-2-sulfonic acid, 2- or3-phosphoglycerate, glucose-6-phosphate or N-cyclohexylsulfamic acid(with formation of the cyclamates) or with other acidic organiccompounds, such as ascorbic acid.

Certain compounds include at least one acidic group that can form anacid-base salt with an inorganic or organic base. Examples of saltsformed from inorganic bases include salts of the presently disclosedcompounds with alkali metals such as potassium and sodium, alkalineearth metals, including calcium and magnesium and the like. Similarly,salts of acidic compounds with an organic base, such as an amine (asused herein terms that refer to amines should be understood to includetheir conjugate acids unless the context clearly indicates that the freeamine is intended) are contemplated, including salts formed with basicamino acids, aliphatic amines, heterocyclic amines, aromatic amines,pyridines, guanidines and amidines. Of the aliphatic amines, the acyclicaliphatic amines, and cyclic and acyclic di- and tri-alkyl amines areparticularly suitable for use in the disclosed compounds. In addition,quaternary ammonium counterions also can be used.

Particular examples of suitable amine bases (and their correspondingammonium ions) for use in the present compounds include, withoutlimitation, pyridine, N,N-dimethylaminopyridine, diazabicyclononane,diazabicycloundecene, N-methyl-N-ethylamine, diethylamine,triethylamine, diisopropylethylamine, mono-, bis- ortris-(2-hydroxyethyl)amine, 2-hydroxy-tert-butylamine,tris(hydroxymethyl)methylamine, N,N-dimethyl-N-(2-hydroxyethyl)amine,tri-(2-hydroxyethyl)amine and N-methyl-D-glucamine. For additionalexamples of “pharmacologically acceptable salts,” see Berge et al., J.Pharm. Sci. 66:1 (1977).

Compounds disclosed herein can be crystallized and can be provided in asingle crystalline form or as a combination of different crystalpolymorphs. As such, the compounds can be provided in one or morephysical form, such as different crystal forms, crystalline, liquidcrystalline or non-crystalline (amorphous) forms. Such differentphysical forms of the compounds can be prepared using, for exampledifferent solvents or different mixtures of solvents forrecrystallization. Alternatively or additionally, different polymorphscan be prepared, for example, by performing recrystallizations atdifferent temperatures and/or by altering cooling rates duringrecrystallization. The presence of polymorphs can be determined by X-raycrystallography, or in some cases by another spectroscopic technique,such as solid phase NMR spectroscopy, IR spectroscopy, or bydifferential scanning calorimetry.

The pharmaceutical compositions can be administered to subjects by avariety of mucosal administration modes, including by oral, rectal,intranasal, intrapulmonary, or transdermal delivery, or by topicaldelivery to other surfaces. Optionally, the compositions can beadministered by non-mucosal routes, including by intramuscular,subcutaneous, intravenous, intra-arterial, intra-articular,intraperitoneal, intrathecal, intracerebroventricular, or parenteralroutes. In other alternative embodiments, the compound can beadministered ex vivo by direct exposure to cells, tissues or organsoriginating from a subject.

To formulate the pharmaceutical compositions, the compound can becombined with various pharmaceutically acceptable additives, as well asa base or vehicle for dispersion of the compound. Desired additivesinclude, but are not limited to, pH control agents, such as arginine,sodium hydroxide, glycine, hydrochloric acid, citric acid, and the like.In addition, local anesthetics (for example, benzyl alcohol),isotonizing agents (for example, sodium chloride, mannitol, sorbitol),adsorption inhibitors (for example, Tween 80 or Miglyol 812), solubilityenhancing agents (for example, cyclodextrins and derivatives thereof),stabilizers (for example, serum albumin), and reducing agents (forexample, glutathione) can be included. Adjuvants, such as aluminumhydroxide (for example, Amphogel, Wyeth Laboratories, Madison, N.J.),Freund's adjuvant, MPL™ (3-O-deacylated monophosphoryl lipid A; Corixa,Hamilton, Ind.) and IL-12 (Genetics Institute, Cambridge, Mass.), amongmany other suitable adjuvants well known in the art, can be included inthe compositions. When the composition is a liquid, the tonicity of theformulation, as measured with reference to the tonicity of 0.9% (w/v)physiological saline solution taken as unity, is typically adjusted to avalue at which no substantial, irreversible tissue damage will beinduced at the site of administration. Generally, the tonicity of thesolution is adjusted to a value of about 0.3 to about 3.0, such as about0.5 to about 2.0, or about 0.8 to about 1.7.

The compound can be dispersed in a base or vehicle, which can include ahydrophilic compound having a capacity to disperse the compound, and anydesired additives. The base can be selected from a wide range ofsuitable compounds, including but not limited to, copolymers ofpolycarboxylic acids or salts thereof, carboxylic anhydrides (forexample, maleic anhydride) with other monomers (for example, methyl(meth)acrylate, acrylic acid and the like), hydrophilic vinyl polymers,such as polyvinyl acetate, polyvinyl alcohol, polyvinylpyrrolidone,cellulose derivatives, such as hydroxymethylcellulose,hydroxypropylcellulose and the like, and natural polymers, such aschitosan, collagen, sodium alginate, gelatin, hyaluronic acid, andnontoxic metal salts thereof. Often, a biodegradable polymer is selectedas a base or vehicle, for example, polylactic acid, poly(lacticacid-glycolic acid) copolymer, polyhydroxybutyric acid,poly(hydroxybutyric acid-glycolic acid) copolymer and mixtures thereof.Alternatively or additionally, synthetic fatty acid esters such aspolyglycerin fatty acid esters, sucrose fatty acid esters and the likecan be employed as vehicles. Hydrophilic polymers and other vehicles canbe used alone or in combination, and enhanced structural integrity canbe imparted to the vehicle by partial crystallization, ionic bonding,cross-linking and the like. The vehicle can be provided in a variety offorms, including fluid or viscous solutions, gels, pastes, powders,microspheres and films for direct application to a mucosal surface.

The compound can be combined with the base or vehicle according to avariety of methods, and release of the compound can be by diffusion,disintegration of the vehicle, or associated formation of waterchannels. In some circumstances, the compound is dispersed inmicrocapsules (microspheres) or nanocapsules (nanospheres) prepared froma suitable polymer, for example, isobutyl 2-cyanoacrylate (see, forexample, Michael et al., J. Pharmacy Pharmacol. 43:1-5, 1991), anddispersed in a biocompatible dispersing medium, which yields sustaineddelivery and biological activity over a protracted time.

The compositions of the disclosure can alternatively contain aspharmaceutically acceptable vehicles substances as required toapproximate physiological conditions, such as pH adjusting and bufferingagents, tonicity adjusting agents, wetting agents and the like, forexample, sodium acetate, sodium lactate, sodium chloride, potassiumchloride, calcium chloride, sorbitan monolaurate, and triethanolamineoleate. For solid compositions, conventional nontoxic pharmaceuticallyacceptable vehicles can be used which include, for example,pharmaceutical grades of mannitol, lactose, starch, magnesium stearate,sodium saccharin, talcum, cellulose, glucose, sucrose, magnesiumcarbonate, and the like.

Pharmaceutical compositions for administering the compound can also beformulated as a solution, microemulsion, or other ordered structuresuitable for high concentration of active ingredients. The vehicle canbe a solvent or dispersion medium containing, for example, water,ethanol, polyol (for example, glycerol, propylene glycol, liquidpolyethylene glycol, and the like), and suitable mixtures thereof.Proper fluidity for solutions can be maintained, for example, by the useof a coating such as lecithin, by the maintenance of a desired particlesize in the case of dispersible formulations, and by the use ofsurfactants. In many cases, it will be desirable to include isotonicagents, for example, sugars, polyalcohols, such as mannitol andsorbitol, or sodium chloride in the composition. Prolonged absorption ofthe compound can be brought about by including in the composition anagent which delays absorption, for example, monostearate salts andgelatin.

In certain embodiments, the compound can be administered in a timerelease formulation, for example in a composition which includes a slowrelease polymer. These compositions can be prepared with vehicles thatwill protect against rapid release, for example a controlled releasevehicle such as a polymer, microencapsulated delivery system orbioadhesive gel. Prolonged delivery in various compositions of thedisclosure can be brought about by including in the composition agentsthat delay absorption, for example, aluminum monostearate hydrogels andgelatin. When controlled release formulations are desired, controlledrelease binders suitable for use in accordance with the disclosureinclude any biocompatible controlled release material which is inert tothe active agent and which is capable of incorporating the compoundand/or other biologically active agent. Numerous such materials areknown in the art. Useful controlled-release binders are materials thatare metabolized slowly under physiological conditions following theirdelivery (for example, at a mucosal surface, or in the presence ofbodily fluids). Appropriate binders include, but are not limited to,biocompatible polymers and copolymers well known in the art for use insustained release formulations. Such biocompatible compounds arenon-toxic and inert to surrounding tissues, and do not triggersignificant adverse side effects, such as nasal irritation, immuneresponse, inflammation, or the like. They are metabolized into metabolicproducts that are also biocompatible and easily eliminated from thebody.

Exemplary polymeric materials for use in the present disclosure include,but are not limited to, polymeric matrices derived from copolymeric andhomopolymeric polyesters having hydrolyzable ester linkages. A number ofthese are known in the art to be biodegradable and to lead todegradation products having no or low toxicity. Exemplary polymersinclude polyglycolic acids and polylactic acids, poly(DL-lacticacid-co-glycolic acid), poly(D-lactic acid-co-glycolic acid), andpoly(L-lactic acid-co-glycolic acid). Other useful biodegradable orbioerodable polymers include, but are not limited to, such polymers aspoly(epsilon-caprolactone), poly(epsilon-aprolactone-CO-lactic acid),poly(epsilon.-aprolactone-CO-glycolic acid), poly(beta-hydroxy butyricacid), poly(alkyl-2-cyanoacrilate), hydrogels, such as poly(hydroxyethylmethacrylate), polyamides, poly(amino acids) (for example, L-leucine,glutamic acid, L-aspartic acid and the like), poly(ester urea),poly(2-hydroxyethyl DL-aspartamide), polyacetal polymers,polyorthoesters, polycarbonate, polymaleamides, polysaccharides, andcopolymers thereof. Many methods for preparing such formulations arewell known to those skilled in the art (see, for example, Sustained andControlled Release Drug Delivery Systems, J. R. Robinson, ed., MarcelDekker, Inc., New York, 1978). Other useful formulations includecontrolled-release microcapsules (U.S. Pat. Nos. 4,652,441 and4,917,893), lactic acid-glycolic acid copolymers useful in makingmicrocapsules and other formulations (U.S. Pat. Nos. 4,677,191 and4,728,721) and sustained-release compositions for water-soluble peptides(U.S. Pat. No. 4,675,189).

The pharmaceutical compositions of the disclosure typically are sterileand stable under sterile conditions of manufacture, storage and use.Sterile solutions can be prepared by incorporating the compound in therequired amount in an appropriate solvent with one or a combination ofingredients enumerated herein, as required, followed by filteredsterilization. Generally, dispersions are prepared by incorporating thecompound and/or other biologically active agent into a sterile vehiclethat contains a basic dispersion medium and the required otheringredients from those enumerated herein. In the case of sterilepowders, methods of preparation include vacuum drying and freeze-dryingwhich yields a powder of the compound plus any additional desiredingredient from a previously sterile-filtered solution thereof. Theprevention of the action of microorganisms can be accomplished byvarious antibacterial and antifungal agents, for example, parabens,chlorobutanol, phenol, sorbic acid, thimerosal, and the like.

In accordance with the various treatment methods of the disclosure, thecompound can be delivered to a subject in a manner consistent withconventional methodologies associated with management of the disorderfor which treatment or prevention is sought. In accordance with thedisclosure herein, a prophylactically or therapeutically effectiveamount of the compound and/or other biologically active agent isadministered to a subject in need of such treatment for a time and underconditions sufficient to prevent, inhibit, and/or ameliorate a selecteddisease or condition or one or more symptom(s) thereof.

The administration of the compound of the disclosure can be for eitherprophylactic or therapeutic purpose. When provided prophylactically, thecompound is provided in advance of any symptom. The prophylacticadministration of the compound serves to prevent or ameliorate anysubsequent disease process. When provided therapeutically, the compoundis provided at (or shortly after) the onset of a symptom of disease orinfection.

For prophylactic and therapeutic purposes, the compound can beadministered to the subject by the oral route or in a single bolusdelivery, via continuous delivery (for example, continuous transdermal,mucosal or intravenous delivery) over an extended time period, or in arepeated administration protocol (for example, by an hourly, daily orweekly, repeated administration protocol). The therapeutically effectivedosage of the compound can be provided as repeated doses within aprolonged prophylaxis or treatment regimen that will yield clinicallysignificant results to alleviate one or more symptoms or detectableconditions associated with a targeted disease or condition as set forthherein. Determination of effective dosages in this context is typicallybased on animal model studies followed up by human clinical trials andis guided by administration protocols that significantly reduce theoccurrence or severity of targeted disease symptoms or conditions in thesubject. Suitable models in this regard include, for example, murine,rat, avian, dog, sheep, porcine, feline, non-human primate, and otheraccepted animal model subjects known in the art. Alternatively,effective dosages can be determined using in vitro models. Using suchmodels, only ordinary calculations and adjustments are required todetermine an appropriate concentration and dose to administer atherapeutically effective amount of the compound (for example, amountsthat are effective to alleviate one or more symptoms of a targeteddisease). In alternative embodiments, an effective amount or effectivedose of the compound may simply inhibit or enhance one or more selectedbiological activities correlated with a disease or condition, as setforth herein, for either therapeutic or diagnostic purposes.

The actual dosage of the compound will vary according to factors such asthe disease indication and particular status of the subject (forexample, the subject's age, size, fitness, extent of symptoms,susceptibility factors, and the like), time and route of administration,other drugs or treatments being administered concurrently, as well asthe specific pharmacology of the compound for eliciting the desiredactivity or biological response in the subject. Dosage regimens can beadjusted to provide an optimum prophylactic or therapeutic response. Atherapeutically effective amount is also one in which any toxic ordetrimental side effects of the compound and/or other biologicallyactive agent is outweighed in clinical terms by therapeuticallybeneficial effects. A non-limiting range for a therapeutically effectiveamount of a compound and/or other biologically active agent within themethods and formulations of the disclosure is about 0.25 mg/kg bodyweight to about 250 mg/kg body weight, such as about 1.0 mg/kg to about100 mg/kg body weight, or about 5 mg/kg to about 50 mg/kg body weight.

Dosage can be varied by the attending clinician to maintain a desiredconcentration at a target site (for example, the lungs or systemiccirculation). Higher or lower concentrations can be selected based onthe mode of delivery, for example, trans-epidermal, rectal, oral,pulmonary, intraosseous, or intranasal delivery versus intravenous orsubcutaneous or intramuscular delivery. Dosage can also be adjustedbased on the release rate of the administered formulation, for example,of an intrapulmonary spray versus powder, sustained release oral versusinjected particulate or transdermal delivery formulations, and so forth.

The compounds disclosed herein may also be co-administered with anadditional therapeutic agent. Such agents include, but are not limitedto, an anti-inflammatory agent, an antimicrobial agent, a matrixmetalloprotease inhibitor, a lipoxygenase inhibitor, a cytokineantagonist, an immunosuppressant, an anti-cancer agent, an anti-viralagent, a cytokine, a growth factor, an immunomodulator, a prostaglandinor an anti-vascular hyperproliferation compound.

The instant disclosure also includes kits, packages and multi-containerunits containing the herein described pharmaceutical compositions,active ingredients, and/or means for administering the same for use inthe prevention and treatment of diseases and other conditions inmammalian subjects. Kits for diagnostic use are also provided. In oneembodiment, these kits include a container or formulation that containsone or more of the compounds described herein. In one example, thiscomponent is formulated in a pharmaceutical preparation for delivery toa subject. The compound is optionally contained in a bulk dispensingcontainer or unit or multi-unit dosage form. Optional dispensing meanscan be provided, for example a pulmonary or intranasal spray applicator.Packaging materials optionally include a label or instruction indicatingfor what treatment purposes and/or in what manner the pharmaceuticalagent packaged therewith can be used.

EXAMPLES Example 1 General Synthesis of a PB Compound

A solution of pyrazine-2-carbaldehyde (4.62 mmol) in absolute ethanol (1ml) is added drop-wise at room temperature over a period of 10 min, withslow stirring, to a solution of NaOH (0.75 mmol) and a ketone (acetone)in a mixture of absolute ethanol and H₂O₂ (14 ml; 1:1 ratio). Thesolution will turn yellow in color followed by formation of a yellowprecipitate within 10 min. The reaction is stirred for 6 h at roomtemperature, after which the yellow solid is removed by filtration andwashed with water; the organic phase is then dried over anhydrous MgSO₄and concentrated in vacuo to give a pale yellow powder representingPB137 at 97% purity.

Example 2 Synthesis of PB Compounds with Acetone

A solution of pyrazine-2-carbaldehyde [or3-aminopyrazine-2-carbaldehyde;6-amino-5-hydroxypyrazine-2-carbaldehyde;5-hydroxy-6-methoxypyrazine-2-carbaldehyde;3-thiocyanatopyrazine-2-carbaldehyde; 5-(chloromethylthio)pyrazine-2-carbaldehyde; 5-acetylpyrazine-2-carbaldehyde;6-(trifluoromethoxy) pyrazine-2-carbaldehyde;5-fluoropyrazine-2-carbaldehyde; 5-(methylthio) pyrazine-2-carbaldehyde;5-(chloromethylthio) pyrazine-2-carbaldehyde;6-tert-butoxypyrazine-2-carbaldehyde; 5-acetylpyrazine-2-carbaldehyde;6-trifluoromethoxypyrazine-2-carbaldehyde;6-amino-5-hydroxypyrazine-2-carbaldehyde;5-hydroxy-6-methoxypyrazine-2-carbaldehyde; or 6-(trifluoromethyl)pyrazine-2-carbaldehyde: (4.62 mmol)] in absolute ethanol (1 ml) isadded drop-wise at room temperature over a period of 10 min, with slowstirring, to a solution of NaOH (0.75 mmol) and acetone in a mixture ofabsolute ethanol and H₂O₂ (14 ml; 1:1 ratio). The solution will turnyellow in color followed by formation of a yellow precipitate within 10min. The reaction is then stirred for 6 h at room temperature, afterwhich the yellow solid is removed by filtration and washed with water;the organic phase is dried over anhydrous Mg504 and concentrated invacuo to give a pale yellow powder representing the desired PB compoundat 97% purity.

Example 3 Synthesis of PB Compounds with Cyclohexanone

A solution of pyrazine-2-carbaldehyde [or3-aminopyrazine-2-carbaldehyde;6-amino-5-hydroxypyrazine-2-carbaldehyde;5-hydroxy-6-methoxypyrazine-2-carbaldehyde;3-thiocyanatopyrazine-2-carbaldehyde; 5-(chloromethylthio)pyrazine-2-carbaldehyde; 5-acetylpyrazine-2-carbaldehyde;6-(trifluoromethoxy) pyrazine-2-carbaldehyde;5-fluoropyrazine-2-carbaldehyde; 5-(methylthio) pyrazine-2-carbaldehyde;5-(chloromethylthio) pyrazine-2-carbaldehyde;6-tert-butoxypyrazine-2-carbaldehyde; 5-acetylpyrazine-2-carbaldehyde;6-trifluoromethoxypyrazine-2-carbaldehyde;6-amino-5-hydroxypyrazine-2-carbaldehyde;5-hydroxy-6-methoxypyrazine-2-carbaldehyde; or 6-(trifluoromethyl)pyrazine-2-carbaldehyde: (4.62 mmol)]) in absolute ethanol (1 ml) isadded drop-wise at room temperature over a period of 10 min, with slowstirring, to a solution of NaOH (0.75 mmol) and cyclohexanone in amixture of absolute ethanol and H₂O₂ (14 ml; 1:1 ratio). The solutionwill turn yellow in color followed by formation of a yellow precipitatewithin 10 min. The reaction is stirred for 6 h at room temperature,after which the yellow solid is removed by filtration and washed withwater; the organic phase is dried over anhydrous MgSO₄ and concentratedin vacuo to give a pale yellow powder representing the desired PBcompound at 97% purity.

Example 4 Purification of PB137

PB137 synthesized at 94-97% purity is dissolved in ethanol at atemperature of 70° C. by adding it slowly using an addition funnel, withslow stirring, until a clear solution forms. Once the clear solution asformed, charcoal is added and the hot reaction mixture is rapidlyfiltered through a bed of Celite. The filtrate is cooled overnight at 4°C. to form pale yellow colored crystals representing PB137 at 99%purity. The purity and identity was confirmed by LC-MS analysis.

Example 5 Synthesis of Thiol Conjugate

N-acetyl-cysteine (NAC) (123 mg, 0.4 mmol) is dissolved in 7 ml of 50%aqueous ethanol and the pH of the resulting solution adjusted to ˜7.8using 1 N NaOH. PB137 (36 mg, 0.2 mmol) is dissolved in 3 ml of ethanol,and then added to the solution described above. The mixture is stirredat ambient temperature under N₂ for 3 h. The solvent is then evaporatedand the crude product purified by reverse phase HPLC using a gradient of0.05% TFA in CH₃CN. The overall yield of PB141 is 97%.

Example 6 Nebulization of PB141

PB141 was dissolved in water or different concentrations of PBS andaerosols were generated using a micropump nebulizer (Buxco ResearchSystems, Wilmington, N.C.) flowing at 10 L of air/min. Aerosol dropletsize was measured with an Andersen cascade impactor. The concentrationof PB141 during a 30-min nebulization period was measured by collectingsamples during nebulization and analyzing them by spectrophotometer inthree independent experiments. Results demonstrated droplet sizes in theoptimum 1-2 μm range (FIG. 1). Nebulization was optimal for a solutionof PB141 in 2% saline, although a formulation in pure water was alsoeffective.

Example 7 TRAP Assay

The anti-oxidant activity of PB141 or PB157 was determined by theability of these compounds to react with the pre-formed radicalmonocation of 2,2′-azinobis-(3-ethylbenzothiazoline)-6-sulfonic acid(ABTS⁺). ABTS (1.8 mmol) was reacted overnight with potassium persulfate(0.63 mmol) in double distilled water, at room temperature in the dark,to generate the dark blue ABTS⁺ radical cation. This radical cation hasa maximum absorption at 734 nm. Immediately prior to the experiment,ABTS⁺ was diluted with absolute ethanol to an absorbance ofapproximately 0.7 at 734 nm. PB141 or PB157 (10 μmol) was added to ABTS⁺(1 ml) and mixed by vortexing. The reaction was allowed to stabilize for5 min and the absorbance was measured. The anti-oxidant activities ofthese compounds were determined by their ability to quench the color ofthe radical cation. Troxol (10 μmol) was used as reference standard.Antioxidant activity of the two compounds was clearly demonstrated.Results for PB141 shown in FIG. 2.

Example 8 FRAP Assay

The antioxidant activity of PB141 or PB157 was determined by ferricreduction/anti-oxidant power (FRAP) assay in which the compounds arereacted with ferric tripyridyltriazine complex. The ferric complex wasprepared at room temperature by reaction of ferric chloride (16.7 mmol)and 2,4,6-trispyridyl-s-triazine (8.33 mmol) in pH 3.6 acetate buffer(0.25 M). The FRAP reagent was used immediately after preparation. PB141or PB157 (10 μmol) was added to the FRAP reagent (1 ml) and mixed byvortexing. The reaction was allowed to stabilize for 5 min and theabsorbance was measured. The antioxidant activities of these compoundswere determined by the ability to reduce the ferric complex to a purpleferrous complex, monitored at 593 nm. Troxol (10 μmol) was used asreference standard. Antioxidant activity of the two compounds was highlysignificant and approximately equal. Results for PB141 shown in FIG. 2.

Example 9 PB141 Exhibits Short Half-Life in the Systemic Circulation

PB141 was dissolved in water as described above and delivered to mice byaerosolization. At 10, 20, 40, 60, 80, 100, 120, 140, 160, 180, 200, 220and 240 min following PB141 delivery blood samples were collected fromthe retro-orbital plexus of mice under light anesthesia. Plasma wasprepared by centrifuging the blood at 2000×g for 5 min and stored frozenat −80±10° C. until analysis. Two hundred microliters of plasma wasspiked with various concentrations of PB141 (to create standard curve)or β-estradiol (internal standard) followed by two volumes of ethylacetate. Samples were mixed for 5 min on a rocker and centrifuged at5,000 rpm for 10 min at room temperature. The supernatant wastransferred to a clean glass tube and dried under nitrogen at 40° C.Samples were reconstituted in 100 μl of mobile phase, and 50 μl wasinjected onto the HPLC system, a Waters 717 UV detector, and a Waters515 pump (Milford, Mass.). A visible wavelength of 430 nm was used todetect PB141 and 280 nm to detect β-estradiol. PB141 separation wasaccomplished by using the isocratic HPLC method. Samples were injectedonto an Apollo reversed-phase C₁₈ column, 150-mm×3.9-mm×5-μm particlesize (Alltech Associates, Deerfield, Ill.). The column was operated at aflow rate of 1 ml/min at room temperature. The mobile phase consisted of1% (wt/vol) citric acid solution, adjusted to pH 3.0 using a 45%potassium hydroxide solution, in HPLC grade water, which was mixed withtetrahydrofuran in a 50:50 (vol/vol) ratio. The solution was filteredthrough a 0.2-μm filter. Rapid disappearance of PB141 from the blood wasobserved (FIG. 4).

Example 10 Nebulized Delivery of PB141 is Non-Toxic to Lung and OtherTissues

PB141 (25 mg/kg or 250 mg/kg) was aerosolized to mice daily for up to 30consecutive days. The standard dose used in efficacy studies is 25 mg/kgfor 1-10 days. At the conclusion of each experiment blood was collectedand the lungs were excised and examined histopathologically for evidenceof injury or toxicity. Serum levels of creatinine and aspartate (AST)and alanine (ALT) aminotransferases were measured using enzyme-linkedimmunosorbent assay (ELISA) kits (R&D Systems, Minneapolis, Minn.)according to the manufacturer's instructions. At the end of 30 days'exposure, other organs were also excised and similarly examined (datanot shown). No evidence of injury or toxicity was found in any study(FIGS. 5A, B).

Example 11 PB141 Upregulates Activity of the Antioxidant TranscriptionFactor Nrf2 and Inhibits the Pro-Inflammatory Transcription Factor NF-κBin Airway Epithelial Cells

BEAS-2B cells were cultured in Dulbecco's modified Eagle's medium (DMEM)containing 10% heat-inactivated fetal bovine serum, penicillin, andstreptomycin (100 IU/ml). Monolayer cultures were treated with differentconcentrations of PB141 for 24 h. Cells were then isolated and theDNA-binding activity of the antioxidant transcription factor Nrf2 wasdetermined. The nuclear concentration of Nrf2 was also determined byWestern blotting. PB141 increased both nuclear localization andDNA-binding activity of Nrf2 in a concentration-dependent manner (FIGS.6A, C). In some experiments monolayer cultures were deprived of serumfor 24 h, pre-treated with different concentrations of PB141 for 1 h,then exposed to LPS for 6 h. Nuclear proteins were prepared and wereused to quantify DNA-binding activity of the p65 subunit of NF-κB. PB141inhibited NF-κB activity in a concentration-dependent manner, withalmost complete inhibition being observed at a concentration of 1 μM(FIG. 6B). In other experiments, no cytotoxicity was observed atconcentrations as high as 10 μM (data not shown).

In other experiments, acute lung injury was induced by intratracheal(i.t.) injection of endotoxin [lipopolysaccharide (LPS)] prepared fromEscherichia coli O111:B6 (Sigma-Aldrich; St. Louis, Mo.). Thirty minuteslater different concentrations of PB141 in isotonic saline werenebulized and delivered into cage air for 30 min using a micropumpnebulizer (Buxco Research Systems, Wilmington, N.C.) fitted at thechamber inlet and flowing at 10 L of air/min. PBS was similarlydelivered as a control. Nuclear proteins were prepared from lung samplesand their concentrations were determined and used to quantifyDNA-binding activity of the p65 subunit of the pro-inflammatorytranscription factor NF-κB. PB141 inhibited the LPS-induced upregulationof NF-κB in a concentration-dependent manner (FIG. 5C).

Example 12 PB141 and PB157 Induce Apoptosis but are not Cytotoxic

To evaluate cell viability, apoptosis, and cytotoxicity, the Apo Tox-GloTriplex assay was used according to the manufacturer's instructions(Promega, Madison, Wis.). Briefly, the BEAS-2B cells were plated at2×10⁴ cells/well in 100 μl medium in an opaque walled, clear-bottomed,96-well plate. After 24 hr culture, they were treated for a furtherindicated time with different concentrations of PB141 or PB157. At theend of the culture period, 20 μl viability/cytotoxicity reagent wasadded to each well, mixed by orbital shaking (300 r.p.m. for 30 s) andincubated for 30 min at 37° C. Fluorescence was then measured withexcitation at 400 nm and emission at 505 nm to assess cell viability,and 485 nm excitation and 520 nm emission to assess cytotoxicity; bothwere quantified as relative fluorescence units (RFU). Then, 100 μlCaspase-Glo 3/7 reagent was added to each well, mixed by orbital shaking(300 r.p.m. for 30 s) and incubated for 30 min at room temperature.Luminescence was measured to assess caspase activation as a marker ofapoptosis and quantified as relative luminescence units. Results forPB141 and PB157 were similar. Both compounds induced apoptosis withoutexhibiting cytotoxicity (data not shown).

Example 13 Nebulization of PB141 Solution Provides Efficient Deliveryinto the Lungs and Prevents Pulmonary Fibrosis

Lung fibrosis was induced by methods previously reported in literatureof the relevant art. Briefly, 50 μl of bleomycin sulfate in saline or0.1 mg of NIEHS crocidolite asbestos (N 10 μm in length) wasadministered intratracheally into anesthetized mice. In some experimentsfibrosis was induced by the following standard X-ray exposure procedure:Anesthetized mice at the age of 10-12 weeks were immobilized, with alead shield excluding all but the thoracic cavity. Animals were thenirradiated with a single dose of 14.5 Gy from a cesium source (J. L.Shepherd and Associates, San Fernando, Calif.) at a dose rate of 1.65Gy/min LD₅₀ for C57BL/6J mice is 14.5 Gy. At this dose, survival issufficient to permit adequate numbers of animals for long-term analyses.

After induction of pulmonary fibrosis using the methods as describedabove, PB141 (25 mg/kg) dissolved in normal saline was delivered for 30min via a micropump nebulizer (Buxco Research Systems, Wilmington, N.C.)fitted at the chamber inlet. After 21 days, bronchoalveolar lavage fluid(BALF) samples were obtained and analyzed for cellular infiltration byhemocytometer and differential staining of cells. Pulmonary fibrosis wasassessed from lung homogenates by estimating total lung collagen contentusing the Sircol Collagen Assay kit (Biocolor) and hydroxyprolinecontent using a hydroxyproline assay kit (BioVision, Mountain View,Calif.) according to the manufacturer's instructions. Lung histologysections were assessed by morphometry, hematoxylin and eosin (H&E)staining, and Masson's trichrome staining. Delivery of the nebulizedPB141 composition effectively prevented inflammatory cell infiltration,collagen production, and myofibroblast differentiation, which indicatedthat effective doses of PB141 were delivered into the lungs. Repeatedpulmonary dosing of the solution (25 mg/kg) significantly reducedpulmonary fibrosis (FIG. 9 shows results for bleomycin induction only).The solution was well tolerated even with intratracheal administration.

Additional in vitro experiments were performed using normal human fetallung fibroblasts (IMR-90; Institute for Medical Research, Camden, N.J.)or fibroblasts grown from mechanically dissociated surgical lung biopsyof histologically normal or usual interstitial pneumonia (UIP) patients.Cells were serum-starved for 24 hr and treated with recombinant 2 mg/mlTGF-β (R&D Systems, Minneapolis, Minn.) for 24 h. In some experimentscells were pretreated with 0.1 to 1 μM PB141 prior to TGF-β treatment.Total cell protein extracts were prepared and assayed for cellproliferation and myofibroblast markers by western blot.Immunohistochemical staining was performed for α-SMA followingtreatment. Pretreatment with PB141 inhibited proliferation (FIG. 7) anddifferentiation to myofibroblasts by human lung fibroblasts, includingthose from UIP patients (FIG. 8).

Example 14 Nebulization of PB141 Solution Provides Efficient Deliveryinto the Lungs and Prevents Lung Injury

Acute lung injury was induced by intratracheal injection of endotoxin(lipopolysaccharide; LPS) prepared from Escherichia coli 0111:B6(Sigma-Aldrich; St. Louis, Mo.) into anesthetized mice. In otherexperiments, systemic sepsis was induced by intraperitoneal injection ofendotoxin. Thirty minutes later PB141 (25 mg/kg) or vehicle (saline) wasdelivered to mice for 30 minutes via a micropump nebulizer (BuxcoResearch Systems, Wilmington, N.C.) fitted at the chamber inlet. Extentof lung injury after 5.5 h and systemic sepsis after 12 h were assessedby measuring lung tissue myeloperoxidase activity, polymorphonuclearneutrophil (PMN) count in bronchoalveolar lavage fluid, lung vascularpermeability, pulmonary edema, and cytokine generation. Lung histologysections were assessed microscopically for evidence of inflammation andinjury following hematoxylin and eosin (H&E) staining.

As shown in FIG. 10, delivery of the PB141 solution via nebulizationeffectively prevented PMN infiltration into the alveolar space, as shownby both decreased PMN count in BAL fluid and decreased lungmyeloperoxidase activity. PB141 also reduced vascular permeability (FIG.11A), edema (FIG. 11B), oxidant stress (FIGS. 10F-H) and cytokinegeneration (FIGS. 10 I-L). Decreased lung injury was seen histologicallyin lungs of mice receiving the nebulized PB141 solution (FIG. 11C).

For additional in vitro studies, after the treatment described abovealveolar macrophages were isolated from the BAL fluid and plated inDMEM+10% FBS. After 1 h, RNA was isolated and expression of thedifferent genes was determined using real-time PCR; results werenormalized to values for the housekeeping genesglyceraldehyde-3-phosphate dehydrogenase (GAPDH) and 9s rRNA.Macrophages from mice treated with PB141 showed decreased transcriptionof inflammatory genes and increased transcription of antioxidant genes(FIG. 13). In other experiments, PMNs were isolated from peripheralblood of endotoxin-treated mice by hetastarch exchange transfusion. PMNadhesion was assessed with the Cytoselect Leukocyte-Endothelium AdhesionAssay kit (CBA-210; Cell Biolabs) and transendothelial PMN migration wasdetermined with the Cytoselect Leukocyte Transmigration Assay kit(CBA-212; Cell Biolabs). Cells from mice treated with PB141 showeddecreased PMN adhesion and transendothelial migration.

Example 15 Nebulization of a PB141 Solution Provides Efficient Deliveryinto the Lungs and Prevents Lung Cancer

A/J mice were injected intraperitoneally on days 1, 3, and 5 with 50mg/kg of 4-methylnitrosamino-1-(3-pyridyl)-1-butanone (NNK; ChemsynScience Laboratories, Lenexa, Kans.) dissolved in saline. The mice werethen held for 8 weeks to allow development of preinvasive lesions:alveolar hyperplasias and adenomas. In some experiments cancer wasinduced by X-ray irradiation as follows: The mice were placed into apolycarbonate cage and separated with hard paper. Whole body irradiationfor systemic damage was performed using a linear accelerator (MEVATRONPRIMUS®; SIEMENS Medical Solutions, CA, USA) that produces 6 MV photons.The linear accelerator was positioned at a source-to-skin distance of100 cm and irradiation was delivered at a dose rate of 3.0 Gy/min. PB141(25 mg/kg) or vehicle (saline) was delivered to mice for 30 min/day foreight weeks via a micropump nebulizer (Buxco Research Systems,Wilmington, N.C.).

Mice were euthanized following the eight-week treatment period. Lunghistology sections were stained by hematoxylin and eosin (H&E). Lunglesions were quantified by determining the incidence and prevalence ofpulmonary pleural surface tumors, counting both the right and left lungsof each mouse. The researcher performing adenoma assessment was blind tothe treatment employed. Hyperplastic and neoplastic lesions of the lungswere scored according to the International Classification of RodentTumors in 6 or 7 sections per lung. Sections were further assessed formorphometry and Ki67 immunohistochemistry. Delivery of PB141significantly (˜40%) inhibited tumor progression, premalignant lungcancer, and cell proliferation in the A/J mouse model (FIG. 14).

For further in vitro studies, human lung adenocarcinoma cell lines(NCI-H661, NCI-H441 and NCIH1299) were obtained from American TypeCulture Collection. Cells were treated with 1 μM NNK for 1 hr. In someexperiments cells were pretreated with 1 to 5 μM PB141 before treatmentwith NNK. Cell proliferation was assessed by BrdU proliferation kit(Roche Applied Science). Apoptosis was assessed by TUNEL assay.Treatment with PB141 significantly decreased cell proliferation andinduced apoptosis in NNK-induced lung adenocarcinoma cells (data notshown).

Example 16 Nebulization of a PB141 Solution Provides Efficient Deliveryinto the Lungs and Prevents COPD

Mice were exposed 5 days per week for 4 wk (sub-acute exposure) to thesmoke of five cigarettes (Reference Cigarette 2R4F without filter;University of Kentucky) administered four times per day with a 30-minsmoke-free interval between exposures. An optimal smoke:air ratio of 1:6was obtained. In preventive studies, tobacco smoke exposure wasparalleled by delivery of a nebulized solution containing PB141 (25mg/kg) or vehicle (saline) via a micropump nebulizer (Buxco ResearchSystems, Wilmington, N.C.). At the conclusion of smoke exposure theextent of lung inflammation was assessed by counting polymorphonuclearneutrophils (PMNs) in bronchoalveolar lavage fluid and measuring lungvascular permeability, edema, pulmonary lymphoid aggregation, andgeneration of inflammatory chemokines and cytokines. Emphysema wasassessed by destruction of alveolar walls, quantitated as thedestructive index (DI), and by enlargement of alveolar spaces,quantitated by the mean linear intercept (Lm). Airway remodeling wasassessed by staining collagen in the airway wall and by measuring theamount of fibronectin. Lung histology sections were assessed forinflammation and injury following hematoxylin and eosin (H&E) staining.Lymphoid aggregates were quantification by morphometric analysis.

As shown in FIG. 18, delivery of a nebulized PB141 solutionsignificantly decreased the cigarette smoke-induced increases ofinflammatory cells in the lungs, pulmonary lymphoid aggregates,generation of inflammatory chemokines and cytokines, airway wallremodeling, development of pulmonary hypertension, and emphysema.Furthermore, administration of PB141 by nebulization improved thephagocytic ability of alveolar macrophages.

For further in vitro studies, bronchial epithelial cells, THP cells(obtained from American Type Culture Collection), and alveolarmacrophages (isolated from bronchial lavage fluid of humans and mice)were cultured and exposed to 10% cigarette smoke extract (CSE) preparedby smoking two cigarettes into RPMI medium according to the FederalTrade Commission (FTC) protocol. In some experiments cells werepretreated with 1 to 5 μM PB141 before the cigarette smoke extracttreatment. Pretreatment with PB141 decreased epithelial cellpermeability, inflammatory chemokine and cytokine production, and ROSgeneration. It also improved the phagocytic ability of mouse and humanalveolar macrophages.

Example 17 Nebulization of a PB141 Solution Provides Efficient Deliveryinto the Lungs and Prevents Asthma

Allergen induced asthma was produced in mice by initial sensitization byintraperitoneal injection of OVA on days 0 and 7 and challenge byintratracheal injection of OVA on even-numbered days 14 through 22.Thirty minutes following each OVA challenge, PB141 (25 mg/kg) or vehicle(saline) was nebulized into the cage air for 30 min. Twenty-four hoursfollowing the last challenge and nebulization. airwayhyperresponsiveness to methacholine challenge was measured noninvasivelyby whole body plethysmography (WBP; Buxco Research Systems, Wilmington,N.C.) and, invasively by computer-controlled ventilator (flexiVent;SCIREQ Inc., Montreal, Canada). Cellular Infiltration into the airspacewas assessed by measuring myeloperoxidase activity in the lung and thenumber of polymorphonuclear neutrophils and eosinophils inbronchoalveolar lavage fluid (BALF). Lung inflammation was assessed byvascular permeability, edema, and cytokine generation. Anti-OVA IgEconcentrations in the serum were measured using an ELISA kit (MDBioproducts, St. Paul, Minn.). Lung histology sections were assessed bymorphometry, with May-Grünwald-Giemsa or Periodic acid-Schiff (PAS)staining used for detection of mucopolysaccharide accumulation, SiriusRed or Masson's trichrome staining for detection of collagen deposition,and hematoxylin and eosin (H&E) staining for assessment of inflammation.Lung collagen content was determined by quantifying soluble collagenwith the Sircol Collagen Assay Kit (Biocolor).

As shown in FIGS. 15-17, nebulized delivery of the PB141 solutionsignificantly suppressed airway hyperresponsiveness while lesseningairway remodeling and mucus accumulation. It suppressed the infiltrationof inflammatory cells into the airspace and lung and attenuated theexpression of cytokines, chemokines, and IgE in BALF and serum. PB141administration also inhibited cytokine generation, iNOS expression, andNO production in lung epithelial cells (BEAS2B) stimulated with 10 ng/mlIFN-γ or IL-4/IL-13 for 6 h.

Example 18 Nebulization of a PB141 Solution Provides Efficient Deliveryinto the Lungs and Prevents Pulmonary hypertension

Pulmonary hypertension was induced in mice by exposing them to chronichypoxia (Fi_(O2) 10%) for 3 weeks. Control mice breathed room air duringthe last 10 days of exposure, PB141 (25 mg/kg) or vehicle (saline) wasnebulized into the cage air for 30 min via a nebulizer.

Pulmonary Delivery of PB141 Reduces Right Ventricular Systolic Pressurein Chronic Hypoxia-Induced Pulmonary Hypertension.

Twenty-four hours following the last PB141 administration, mice wereanesthetized, and the right internal jugular vein of each mouse wassurgically exposed and cannulated with a pressure transducer that wasadvanced to record right ventricular systolic pressure (RVSP), which iselevated in pulmonary hypertension. Pressure increases weresignificantly smaller in PB141-treated mice, as were pulmonary arterialpressure and pulmonary vascular resistance. The heart was then excisedand the right ventricle was separated from the left ventricle (includingthe septum). Each ventricle was weighted separately. Pulmonaryhypertension induces right ventricular hypertrophy, but PB141 treatmentsignificantly reduced the increase in ratio of right ventricular weightto that of the left ventricle plus septum (FIG. 19).

Pulmonary Delivery of PB141 Reduces Vascular Remodeling in ChronicHypoxia-Induced Pulmonary Hypertension.

Twenty-four hours following the last PB141 administration, lung sampleswere obtained. Immunostaining for α-SMA, a key marker in pulmonaryhypertension, was performed in paraffin sections of lung and thesections were examined microscopically. The number of α-SMA-positiveacinar blood vessels was quantified and the number demonstrating no,partial, or full muscularization was determined, as was the median wallthickness of vessels positive for α-SMA. All these measures of vascularwall remodeling in small pulmonary vessels, the pathophysiologyunderlying pulmonary hypertension, were reduced by PB141 treatment (FIG.20).

In view of the many possible embodiments to which the principles of thedisclosed invention may be applied, it should be recognized that theillustrated embodiments are only preferred examples of the invention andshould not be taken as limiting the scope of the invention.

1-8. (canceled)
 9. A compound, or a pharmaceutically acceptable salt orester thereof, comprising an adduct of a hydrophilic thiol and an enonethat comprises at least two N-heterocycles.
 10. A compound, or apharmaceutically acceptable salt or ester thereof, having a structureof:

wherein

represents a single bond; A is CH(S—R⁵), wherein R⁵ is a peptide, aminoacid, amino acid derivative, optionally-substituted alkyl,optionally-substituted alkenyl, optionally-substituted alkynyl,optionally-substituted cycloalkyl, or optionally-substitutedcycloalkenyl; and X¹ and X² are each independently anoptionally-substituted N-heterocycle; or

wherein

represents a single bond; A is CH(S—R⁵), wherein R⁵ is a peptide, aminoacid, amino acid derivative, optionally-substituted alkyl,optionally-substituted alkenyl, optionally-substituted alkynyl,optionally-substituted cycloalkyl, or optionally-substitutedcycloalkenyl; X¹ and X² are each independently an optionally-substitutedN-heterocycle; and R¹, R², and R³ are each independently C or N; or

wherein

represents a single bond; A is CH(S—R⁵), wherein R⁵ is a peptide, aminoacid, amino acid derivative, optionally-substituted alkyl,optionally-substituted alkenyl, optionally-substituted alkynyl,optionally-substituted cycloalkyl, or optionally-substitutedcycloalkenyl; X¹ and X² are each independently an optionally-substitutedN-heterocycle; and R¹ is C or N; or

wherein

represents a single bond; A is CH(S—R⁵), wherein R⁵ is a peptide, aminoacid, amino acid derivative, optionally-substituted alkyl,optionally-substituted alkenyl, optionally-substituted alkynyl,optionally-substituted cycloalkyl, or optionally-substitutedcycloalkenyl; R¹ and R² are each independently C or N; X¹ and X² areeach independently an optionally-substituted N-heterocycle.
 11. Thecompound of claim 10, wherein X¹ has a structure of:

and X² has a structure of:

wherein Z¹, Z², and Z³ are each independently C or N, provided that atleast one of Z¹, Z², or Z³ is N; and Y¹, Y², Y³, Y⁴ and Y⁵ are eachindependently H, optionally-substituted alkyl, amino, hydroxyl,optionally-substituted alkoxy, optionally-substituted thiol, acyl, orhalogen.
 12. The compound of claim 10, wherein the compound has astructure of:


13. The compound of 12, wherein the compound has a structure of:

wherein Y², Y³, Y⁴ and Y⁵ are each independently H,optionally-substituted alkyl, amino, hydroxyl, optionally-substitutedalkoxy, optionally-substituted thiol, acyl, or halogen. 14-15.(canceled)
 16. The compound of claim 12, wherein X¹ and X² are eachoptionally-substituted pyrazinyl or optionally-substituted pyrimidinyl.17. The compound of claim 16, wherein X¹ and X² are each the same. 18.The compound of claim 16, wherein X¹ and X² are each different.
 19. Thecompound of claim 12, wherein R⁵ is an acylamino-substitutedcarboxylalkyl, a sulfonate-substituted alkyl, or anacylamino-substituted amido.
 20. The compound of claim 12, wherein —S—R⁵is a derivative of N-acetylcysteine, 2-mercaptoethane sulfonate, orglutathione.
 21. A pharmaceutical composition comprising a compound ofclaim 10, and at least one pharmaceutically acceptable excipient. 22.The pharmaceutical composition of claim 21, wherein the composition isin the form of an aerosol.
 23. The pharmaceutical composition of claim21, wherein the composition is in the form of a dry powder.
 24. A methodfor treating a pulmonary disease in a subject comprising administeringto the subject in need thereof a therapeutically effective amount of acompound, or a pharmaceutically acceptable salt or ester thereof, havinga structure of:X¹-L-X² wherein L is a linking moiety comprising an enone; and X¹ and X²are each independently an optionally-substituted N-heterocycle.
 25. Themethod of claim 24, wherein the compound is administered to the subjectvia inhalation.
 26. The method of claim 24, wherein the compound isadministered via direct pulmonary delivery.
 27. A method for treating apulmonary disease in a subject comprising administering to the subjectin need thereof a therapeutically effective amount of a pharmaceuticalcomposition of claim
 21. 28. The method of claim 24, wherein thepulmonary disease is pulmonary fibrosis, chronic obstructive pulmonarydisease (COPD), asthma, cystic fibrosis, acute lung injury (ALI), acuterespiratory distress syndrome, pulmonary hypertension, lung cancer, orpulmonary manifestations of cystic fibrosis.
 29. A method for treatingan ischemia-reperfusion condition in a subject comprising administeringto the subject in need thereof a therapeutically effective amount of acompound, or a pharmaceutically acceptable salt or ester thereof, havinga structure of:X¹-L-X² wherein L is a linking moiety comprising an enone; and X¹ and X²are each independently an optionally-substituted N-heterocycle.
 30. Amethod for treating an ischemia-reperfusion condition in a subjectcomprising administering to the subject in need thereof atherapeutically effective amount of a pharmaceutical composition ofclaim
 21. 31. The method of claim 29, wherein the ischemia andreperfusion is consequent to transplanting of an organ in the subject.32. The method of claim 31, wherein the compound is administered to adonor prior to removal of the organ.
 33. The method of claim 31, whereinthe compound is provided to the transplanted organ between the time ofremoval from a donor and placement in a recipient.
 34. The method ofclaim 31, wherein the organ is a lung.
 35. A method of inhibiting NF-κBactivity in a subject, inhibiting lung fibroblast proliferation in asubject, inhibiting myofibroblast differentiation in a subject,inhibiting an oxidizing agent in lung tissue of a subject, amelioratingor preventing acute or chronic rejection of a transplanted organ in asubject, increasing a subject's endogenous antioxidant activity viaupregulation of the activity of the transcription factor Nrf2,inhibiting pulmonary collagen deposition in a subject, diminishing theinflammatory response to allergen in a subject, diminishing theinflammatory response to an inflammatory, irritating, or cytotoxic agentin a subject, diminishing allergen-induced excessive response tobronchoconstrictors in a subject, diminishing allergen-induced airwayremodeling in a subject, or diminishing hypoxia-induced remodeling ofthe pulmonary vasculature in a subject, comprising administering to thesubject in need thereof a therapeutically effective amount of acompound, or a pharmaceutically acceptable salt or ester thereof, havinga structure of:X¹-L-X² wherein L is a linking moiety comprising an enone; and X¹ and X²are each independently an optionally-substituted N-heterocycle. 36-42.(canceled)
 43. A method for decreasing proliferation and inducingapoptosis in lung cancer cells, comprising contacting the cells with aneffective amount of a compound, or a pharmaceutically acceptable salt orester thereof, having a structure of:X¹-L-X² wherein L is a linking moiety comprising an enone; and X¹ and X²are each independently an optionally-substituted N-heterocycle.
 44. Amethod for improving the phagocytotic ability of alveolar macrophages,comprising contacting the microphages with an effective amount of acompound, or a pharmaceutically acceptable salt or ester thereof, havinga structure of:X¹-L-X² wherein L is a linking moiety comprising an enone; and X¹ and X²are each independently an optionally-substituted N-heterocycle. 45-49.(canceled)
 50. A method for treating a pulmonary disease in a subjectcomprising administering to the subject in need thereof atherapeutically effective amount of a compound of claim
 10. 51. A methodfor treating a pulmonary disease in a subject comprising administeringto the subject in need thereof a therapeutically effective amount of acompound of claim
 12. 52. The compound of claim 13, wherein R⁵ is anacylamino-substituted carboxylalkyl, a sulfonate-substituted alkyl, oran acylamino-substituted amido.
 53. The compound of claim 13, wherein—S—R⁵ is a derivative of N-acetylcysteine, 2-mercaptoethane sulfonate,or glutathione.